All topical and oral Glutathione containing products should be registered under the Borderline Products Regulatory Division/NMRA.

Intravenous (IV) products are not registered under the Borderline Products Regulatory Division and intravenous Glutathione containing products are not recommended as skin lightening agents. (31st BPEC-2021/02/16)

NMRA prior approval should be obtained for advertisement purpose of all such products.

Therefore, you are requested to initiate the product registration and follow the below instructions.

1. Profile creation

2. Submission for product classification

3. Obtained the Sample Import Licenses

4. Submit the registration dossier

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(Date: 09 March 2021)