NDC 11822-0551 Body
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 11822-0551?
What are the uses for Body?
Which are Body UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Body 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:
- TALC (UNII: 7SEV7J4R1U)
- ACACIA (UNII: 5C5403N26O)
- EUCALYPTOL (UNII: RV6J6604TK)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- THYMOL (UNII: 3J50XA376E)
- ZINC STEARATE (UNII: H92E6QA4FV)
What is the NDC to RxNorm Crosswalk for Body?
- 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
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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".