NDC 72102-047 Maketa Sunscreen With Aloe Vera Spf 30

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:
72102-047
Proprietary Name:
Maketa Sunscreen With Aloe Vera Spf 30
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
72102
Start Marketing Date: [9]
06-01-2018
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)

Code Structure Chart

Product Details

What is NDC 72102-047?

The NDC code 72102-047 is assigned by the FDA to the product Maketa Sunscreen With Aloe Vera Spf 30 which is product labeled by Mak�ta� Sunscreen Lotion With Aloe Vera Spf 30. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 72102-047-06 177 ml in 1 tube , 72102-047-18 532 ml in 1 bottle, pump . 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 Maketa Sunscreen With Aloe Vera Spf 30?

*Apply liberally 15 minutes before sun exposure.*Use a water resistant sunscreen if swimming or sweating.*Reapply at least every 2 hours.*Children under 6 months: Ask a Doctor

Which are Maketa Sunscreen With Aloe Vera Spf 30 UNII Codes?

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

Which are Maketa Sunscreen With Aloe Vera Spf 30 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:

* Please review the disclaimer below.

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".