NDC 69677-010 Vitacin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69677 - Mas Management Group Inc.
- 69677-010 - Vitacin
Product Packages
NDC Code 69677-010-01
Package Description: 120 g in 1 PACKAGE
Product Details
What is NDC 69677-010?
What are the uses for Vitacin?
Which are Vitacin UNII Codes?
The UNII codes for the active ingredients in this product are:
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- CAPSAICIN (UNII: S07O44R1ZM)
- CAPSAICIN (UNII: S07O44R1ZM) (Active Moiety)
Which are Vitacin 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:
- WATER (UNII: 059QF0KO0R)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CHONDROITIN SULFATE (BOVINE) (UNII: 6IC1M3OG5Z)
- EMU OIL (UNII: 344821WD61)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- LAURETH-7 (UNII: Z95S6G8201)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- PEG-100 STEARATE (UNII: YD01N1999R)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TROLAMINE (UNII: 9O3K93S3TK)
- UREA (UNII: 8W8T17847W)
What is the NDC to RxNorm Crosswalk for Vitacin?
- RxCUI: 1099896 - capsaicin 0.0375 % / menthol 5 % / methyl salicylate 20 % Topical Cream
- RxCUI: 1099896 - capsaicin 0.375 MG/ML / menthol 50 MG/ML / methyl salicylate 200 MG/ML Topical Cream
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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".