NDC 69822-101 Ice Quake Plus
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 69822-101?
What are the uses for Ice Quake Plus?
Which are Ice Quake Plus 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)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
Which are Ice Quake Plus 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:
- HYPROMELLOSE 2910 (10000 MPA.S) (UNII: 0HO1H52958)
- GLYCERIN (UNII: PDC6A3C0OX)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- CARBOMER HOMOPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: F68VH75CJC)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Ice Quake Plus?
- RxCUI: 1990885 - camphor 3.1 % / menthol 10 % / methyl salicylate 10 % Topical Cream
- RxCUI: 1990885 - camphor 31 MG/ML / menthol 100 MG/ML / methyl salicylate 100 MG/ML Topical Cream
- RxCUI: 1990890 - Ice Quake 3.1 % / 10 % / 10 % Topical Cream
- RxCUI: 1990890 - camphor 31 MG/ML / menthol 100 MG/ML / methyl salicylate 100 MG/ML Topical Cream [Ice Quake]
- RxCUI: 1990890 - Ice Quake (camphor 3.1 % / menthol 10 % / methyl salicylate 10 % ) 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".