NDC 73204-101 Mother Spf - Daily Face And Body Spf30 Broad Spectrum

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
73204-101
Proprietary Name:
Mother Spf - Daily Face And Body Spf30 Broad Spectrum
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Mother Sun Protection Factor Pty Ltd
Labeler Code:
73204
Start Marketing Date: [9]
08-01-2019
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 73204-101-11

Package Description: 120 g in 1 TUBE

Product Details

What is NDC 73204-101?

The NDC code 73204-101 is assigned by the FDA to the product Mother Spf - Daily Face And Body Spf30 Broad Spectrum which is product labeled by Mother Sun Protection Factor Pty Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 73204-101-11 120 g in 1 tube . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Mother Spf - Daily Face And Body Spf30 Broad Spectrum?

Apply generously 15 minutes before sun exposure.Reapply after 80 minutes of swimming or sweating.Reapply immediately after towel drying.Reapply at least every 2 hours.Children under 6 months of age: Ask a doctor.

Which are Mother Spf - Daily Face And Body Spf30 Broad Spectrum UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Mother Spf - Daily Face And Body Spf30 Broad Spectrum Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".