NDC 52920-134 Ice Cold Analgesic
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 52920 - Singhfam Corporation
- 52920-134 - Ice Cold Analgesic
Product Packages
NDC Code 52920-134-49
Package Description: 227 g in 1 BOTTLE, PLASTIC
Product Details
What is NDC 52920-134?
What are the uses for Ice Cold Analgesic?
Which are Ice Cold Analgesic UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
Which are Ice Cold Analgesic 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:
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- CARBOMER HOMOPOLYMER TYPE B (ALLYL SUCROSE CROSSLINKED) (UNII: Z135WT9208)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
What is the NDC to RxNorm Crosswalk for Ice Cold Analgesic?
- RxCUI: 1661018 - camphor 0.5 % / menthol 2 % Topical Gel
- RxCUI: 1661018 - camphor 0.005 MG/MG / menthol 0.02 MG/MG Topical Gel
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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".