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  4. NDC Product Code: 77338-403 Astonea Medicated Body Powder Powder

NDC 77338-403 Astonea Medicated Body Powder Powder

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 77338-403?
  4. Astonea Medicated Body Powder Powder Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
77338-403
Proprietary Name:
Astonea Medicated Body Powder Powder
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Astonea Labs Private Limited
Labeler Code:
77338
Product Label ID:
e69b4924-313b-0ea5-e053-2995a90a616d
Start Marketing Date: [9]
10-05-2021
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

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Product Details

What is NDC 77338-403?

The NDC code 77338-403 is assigned by the FDA to the product Astonea Medicated Body Powder Powder which is product labeled by Astonea Labs Private Limited. The product's dosage form is . The product is distributed in a single package with assigned NDC code 77338-403-10 283 g in 1 bottle . 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 Astonea Medicated Body Powder Powder?

Adults and children 2 years and older, apply freely up to 3 or 4 times dailyunder 2 years: ask a doctor before usingfor best results, dry skin thoroughly before use

Which are Astonea Medicated Body Powder Powder UNII Codes?

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

Which are Astonea Medicated Body Powder Powder 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:

What is the NDC to RxNorm Crosswalk for Astonea Medicated Body Powder Powder?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 577232 - menthol 0.15 % / zinc oxide 1 % Topical Powder
  • RxCUI: 577232 - menthol 0.0015 MG/MG / zinc oxide 0.01 MG/MG Topical Powder
  • RxCUI: 577232 - Menthol 0.0015 MG/MG / ZNO 0.01 MG/MG Topical Powder

* 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".