NDC 55910-407 Anti-itch
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 55910 - Dolgencorp, Inc.
- 55910-407 - Anti-itch
Product Packages
NDC Code 55910-407-03
Package Description: 28 g in 1 TUBE
Product Details
What is NDC 55910-407?
What are the uses for Anti-itch?
Which are Anti-itch UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5)
- PRAMOXINE (UNII: 068X84E056) (Active Moiety)
Which are Anti-itch 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- EUCALYPTOL (UNII: RV6J6604TK)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- MINERAL OIL (UNII: T5L8T28FGP)
- PETROLATUM (UNII: 4T6H12BN9U)
- PPG-1 TRIDECETH-6 (UNII: 1K7417JX6Q)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- STEARETH-21 (UNII: 53J3F32P58)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- THYMOL (UNII: 3J50XA376E)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TROLAMINE (UNII: 9O3K93S3TK)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Anti-itch?
- RxCUI: 1116155 - menthol 1 % / pramoxine HCl 1 % Topical Cream
- RxCUI: 1116155 - menthol 10 MG/ML / pramoxine hydrochloride 10 MG/ML Topical Cream
- RxCUI: 1116155 - menthol 1 % / pramoxine hydrochloride 1 % Topical Cream
* Please review the disclaimer below.
[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".