NDC 77338-013 Menthol And Zinc Oxide
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 77338 - Astonea Labs Private Limited
- 77338-013 - Menthol And Zinc Oxide
Product Packages
NDC Code 77338-013-23
Package Description: 113 g in 1 TUBE
Product Details
What is NDC 77338-013?
What are the uses for Menthol And Zinc Oxide?
Which are Menthol And Zinc Oxide 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 Menthol And Zinc Oxide 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- LANOLIN (UNII: 7EV65EAW6H)
- LIGHT MINERAL OIL (UNII: N6K5787QVP)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- THYMOL (UNII: 3J50XA376E)
- PETROLATUM (UNII: 4T6H12BN9U)
What is the NDC to RxNorm Crosswalk for Menthol And Zinc Oxide?
- RxCUI: 2123045 - menthol 0.44 % / zinc oxide 20.6 % Topical Ointment
- RxCUI: 2123045 - menthol 0.0044 MG/MG / zinc oxide 0.206 MG/MG Topical Ointment
- RxCUI: 2123045 - Menthol 0.0044 MG/MG / ZNO 0.206 MG/MG Topical Ointment
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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".