NDC 59779-051 Cvs Soothing Itch Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 59779 - Cvs Pharmacy
- 59779-051 - Cvs Soothing Itch Relief
Product Packages
NDC Code 59779-051-37
Package Description: 200 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 59779-051?
What are the uses for Cvs Soothing Itch Relief?
Which are Cvs Soothing Itch Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Cvs Soothing Itch Relief 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:
- WATER (UNII: 059QF0KO0R)
- CARBOMER 1342 (UNII: 809Y72KV36)
- GLYCERIN (UNII: PDC6A3C0OX)
- OATMEAL (UNII: 8PI54V663Y)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- PROPYLENE GLYCOL DICAPRYLATE/DICAPRATE (UNII: O4446S9CRA)
- ISOPROPYL STEARATE (UNII: 43253ZW1MZ)
- CETYL ESTERS WAX (UNII: D072FFP9GU)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- DIMETHICONE 350 (UNII: 2Y53S6ATLU)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- ANHYDROUS TRISODIUM CITRATE (UNII: RS7A450LGA)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- EVENING PRIMROSE OIL (UNII: 3Q9L08K71N)
- POLYOXYL 40 CASTOR OIL (UNII: 4ERD2076EF)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
What is the NDC to RxNorm Crosswalk for Cvs Soothing Itch Relief?
- RxCUI: 1098347 - menthol 0.1 % Topical Lotion
- RxCUI: 1098347 - menthol 1 MG/ML Topical Lotion
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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".