NDC 73428-1002 Body Merry Spf 15 Sunscreen Cream

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:
73428-1002
Proprietary Name:
Body Merry Spf 15 Sunscreen Cream
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Body Merry, Llc
Labeler Code:
73428
Start Marketing Date: [9]
11-14-2019
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 73428-1002-1

Package Description: 60 mL in 1 TUBE

Product Details

What is NDC 73428-1002?

The NDC code 73428-1002 is assigned by the FDA to the product Body Merry Spf 15 Sunscreen Cream which is product labeled by Body Merry, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 73428-1002-1 60 ml 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 Body Merry Spf 15 Sunscreen Cream?

Apply every morning as a daily moisturizer. Apply generously and evenly 15 minutes before sun exposure. Reapply at least every two hours. Use a water-resistant sunscreen if swimming or sweating. Children under six months of age: consult a doctor before use.

Which are Body Merry Spf 15 Sunscreen Cream UNII Codes?

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

Which are Body Merry Spf 15 Sunscreen Cream 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".