NDC 41250-797 Anti-itch
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 41250 - Meijer
- 41250-797 - Anti-itch
Product Packages
NDC Code 41250-797-06
Package Description: 222 mL in 1 BOTTLE
Product Details
What is NDC 41250-797?
What are the uses for Anti-itch?
Which are Anti-itch UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (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:
- CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- PEG-8 STEARATE (UNII: 2P9L47VI5E)
- PEG-100 STEARATE (UNII: YD01N1999R)
- PETROLATUM (UNII: 4T6H12BN9U)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Anti-itch?
- RxCUI: 200176 - camphor 0.5 % / menthol 0.5 % Topical Lotion
- RxCUI: 200176 - camphor 5 MG/ML / menthol 5 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".