NDC 69739-070 Atobos Baby Aqua Soothing
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69739 - 1004laboratory
- 69739-070 - Atobos Baby Aqua Soothing
Product Packages
NDC Code 69739-070-01
Package Description: 160 mL in 1 CARTON
Product Details
What is NDC 69739-070?
What are the uses for Atobos Baby Aqua Soothing?
Which are Atobos Baby Aqua Soothing UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALLANTOIN (UNII: 344S277G0Z)
- ALLANTOIN (UNII: 344S277G0Z) (Active Moiety)
Which are Atobos Baby Aqua Soothing 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:
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- GLYCERIN (UNII: PDC6A3C0OX)
What is the NDC to RxNorm Crosswalk for Atobos Baby Aqua Soothing?
- RxCUI: 1442087 - allantoin 0.5 % Topical Gel
- RxCUI: 1442087 - allantoin 0.005 MG/MG Topical Gel
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[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".