NDC 69706-0204 Fast Relief Reumacetin
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 69706-0204?
What are the uses for Fast Relief Reumacetin?
Which are Fast Relief Reumacetin UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Fast Relief Reumacetin 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:
- ACRYLAMIDE (UNII: 20R035KLCI)
- AMINO ACIDS, WHEAT (UNII: 0370GZL32F)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- COMFREY LEAF (UNII: DG4F8T839X)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- GLUCOSAMINE (UNII: N08U5BOQ1K)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- MINERAL OIL (UNII: T5L8T28FGP)
- PANTHENOL (UNII: WV9CM0O67Z)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- TROLAMINE (UNII: 9O3K93S3TK)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Fast Relief Reumacetin?
- RxCUI: 1673877 - menthol 2.5 % / methyl salicylate 15 % Topical Cream
- RxCUI: 1673877 - menthol 25 MG/ML / methyl salicylate 150 MG/ML Topical Cream
- RxCUI: 1744388 - Reumacetin 2.5 % / 15 % Topical Cream
- RxCUI: 1744388 - menthol 25 MG/ML / methyl salicylate 150 MG/ML Topical Cream [Reumacetin]
- RxCUI: 1744388 - Reumacetin (menthol 2.5 % / methyl salicylate 15 % ) 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".