NDC 82988-101 Ice Blue Pain Alleviating Rub
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 82988 - Lemisol Corporation
- 82988-101 - Ice Blue Pain Alleviating Rub
Product Packages
NDC Code 82988-101-08
Package Description: 226.7 g in 1 JAR
NDC Code 82988-101-16
Package Description: 453.5 g in 1 JAR
Product Details
What is NDC 82988-101?
What are the uses for Ice Blue Pain Alleviating Rub?
Which are Ice Blue Pain Alleviating Rub UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (Active Moiety)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
- CAMPHOR (NATURAL) (UNII: N20HL7Q941)
- CAMPHOR (NATURAL) (UNII: N20HL7Q941) (Active Moiety)
Which are Ice Blue Pain Alleviating Rub 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:
- ALCOHOL (UNII: 3K9958V90M)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- WATER (UNII: 059QF0KO0R)
- TROLAMINE (UNII: 9O3K93S3TK)
What is the NDC to RxNorm Crosswalk for Ice Blue Pain Alleviating Rub?
- RxCUI: 2624202 - camphor 0.3 % / menthol 2.5 % / methyl salicylate 2.2 % Topical Gel
- RxCUI: 2624202 - camphor 0.003 MG/MG / menthol 0.025 MG/MG / methyl salicylate 0.022 MG/MG Topical Gel
- RxCUI: 2624203 - camphor 3 % / menthol 5 % / methyl salicylate 8 % Topical Spray
- RxCUI: 2624203 - camphor 30 MG/ML / menthol 50 MG/ML / methyl salicylate 80 MG/ML Topical Spray
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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".