71.100.70 - Cosmetics. Toiletries

This document specifies a procedure for evaluating the water resistance retention percentage, by comparing the sun protection factor (SPF) before water immersion (hereafter referred to as the "static" SPF) and after a fixed period of water immersion (hereafter referred to as the "wet" SPF).

This document specifies requirements and test methods for total digestible fluoride content and a
minimum soluble fluoride release potential in dental varnishes containing fluoride, intended for use
in the oral cavity directly on the outer surfaces of teeth and fillings. It also specifies packaging and
labelling requirements, including the instructions for use. This document covers fluoride varnishes to
be applied by dental health care workers.

This document specifies requirements and test methods for the physical properties of powered
toothbrushes in order to promote the safety of these products for their intended use.
There are different technologies of powered toothbrushes. Common features of those powered
toothbrushes to which this document applies are:
— a battery;
— a motor;
— a mechanical or magnetic drive system;
— a moving brush head with tufted filaments.
Powered toothbrushes can have a moving brush head with differen...view more

This document specifies a procedure for evaluating the water resistance retention percentage, by comparing the sun protection factor (SPF) before water immersion (hereafter referred to as the "static" SPF) and after a fixed period of water immersion (hereafter referred to as the "wet" SPF).

This document gives guidance for the enumeration and/or detection of microorganisms present in a cosmetic product that is impregnated or coated onto a substrate (i.e. wipes and masks) where sampling and microbiological influence of the manufactured product presents particular challenges in terms of microbiological sampling and testing.
The principle of this document can also be applied to test similar products (e.g. cushion, impregnated sponge, etc.) or applicators (e.g. brush, puff, sponge, et...view more

This document specifies a procedure of water immersion for the in vivo determination of the water resistance of sunscreen products.
This document is applicable to products intended to be placed in contact with human skin including any component able to absorb, reflect or scatter UV rays and which, in addition, are designed to be less readily removed from the skin by water and/or during water immersion. It is intended to be read in conjunction with ISO 24444.

This document specifies a method for the simultaneous determination of the total alkali content and the total fatty matter content of soaps (including liquid soaps), excluding compounded products.

This document specifies a procedure of water immersion for the in vivo determination of the water resistance of sunscreen products. This document is applicable to products intended to be placed in contact with human skin including any component able to absorb, reflect or scatter UV rays and which, in addition, are designed to be less readily removed from the skin by water and/or during water immersion. It is intended to be read in conjunction with ISO 24444.

EN-ISO 28399 specifies requirements and test methods for external tooth bleaching products. These products are intended for use in the oral cavity, either by professional application (in-office tooth bleaching products) or consumer application (professional or non-professional home use of tooth bleaching products), or both. It also specifies requirements for their packaging, labelling and manufacturer’s instructions for use.This document is not applicable to tooth bleaching products:- specified ...view more

This document specifies requirements and test methods for external tooth bleaching products. These products are intended for use in the oral cavity, either by professional application (in-office tooth bleaching products) or consumer application (professional or non-professional home use of tooth bleaching products), or both. It also specifies requirements for their packaging, labelling and manufacturer's instructions for use.
This document is not applicable to tooth bleaching products:
— speci...view more

This standard specifies a method for the in vivo determination of the sun protectionfactor (SPF) of sunscreen products. It is applicable to products that containany component able to absorb, reflect or scatter ultraviolet (UV) rays and whichare intended to be placed in contact with human skin.This document provides abasis for the evaluation of sunscreen products for the protection of human skinagainst erythema induced by solar ultraviolet rays.

This standard describes the industry best practices to address the concentration of extracts which is related to ISO 16128-2:2017, 4.2. Evaporation of solvents to dryness it not addressed in this document. This document aims to delineate the cases when an extract is produced and, afterwards the mixture of evaporated solvents used, regardless of the categories, are partially evaporated. The producer of the extract can utilize different approaches (e.g. measurement by instrumentation, characteriza...view more

This standard describes additional information to use with ISO 16128-2 for the special situation of hydrolates. It clarifies the method of determining the organic index in the absence of measurement of the quantity of water introduced.

This document defines a global approach for the validation of a quantitative analytical method, based on the construction and interpretation of an accuracy profile, and specifies its characterization procedure. This procedure is particularly applicable for internal validation in a cosmetic testing laboratory, but its scope can be extended to the interpretation of data collected for an interlaboratory study designed according to the recommendations of the ISO 5725-1. It does not apply to microbio...view more

This document specifies a method for the in vivo determination of the sun protection factor (SPF) of sunscreen products. It is applicable to products that contain any component able to absorb, reflect or scatter ultraviolet (UV) rays and which are intended to be placed in contact with human skin.
This document provides a basis for the evaluation of sunscreen products for the protection of human skin against erythema induced by solar ultraviolet rays.

This document specifies a method for the in vivo determination of the sun protection factor (SPF) of sunscreen products. It is applicable to products that contain any component able to absorb, reflect or scatter ultraviolet (UV) rays and which are intended to be placed in contact with human skin. This document provides a basis for the evaluation of sunscreen products for the protection of human skin against erythema induced by solar ultraviolet rays.

This Standard gives guidelines for the stability testing of cosmetic products. It reviews readily available bibliographic references that provide a resource for the assessment of the stability of cosmetic products. This review of the available guidelines that assess the stability of cosmetic products can serve as a technical/scientific framework to identify the most suitable methods for the assessment of the stability of cosmetic products. This document does not aim to specify the conditions, pa...view more

This document specifies a procedure for the interpretation of data generated by the preservation
efficacy test or by the microbiological risk assessment, or both, when evaluating the overall
antimicrobial protection of a cosmetic product.
It comprises:
— a preservation efficacy test;
— a procedure for evaluating the overall antimicrobial protection of a cosmetic product that is not
considered low risk, based on a risk assessment described in ISO 29621.
The preservation efficacy test is a ...view more

This document describes additional information to use with ISO 16128-2 for the special situation of hydrolates. It clarifies the method of determining the organic index in the absence of measurement of the quantity of water introduced.

This document describes the industry best practices to address the concentration of extracts which is related to ISO 16128-2:2017, 4.2. Evaporation of solvents to dryness it not addressed in this document. This document aims to delineate the cases when an extract is produced and, afterwards the mixture of evaporated solvents used, regardless of the categories, are partially evaporated. The producer of the extract can utilize different approaches (e.g. measurement by instrumentation, characteriza...view more