NDC 49035-333 Equate Medicated Dry And Itch
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What is NDC 49035-333?
What are the uses for Equate Medicated Dry And Itch?
Which are Equate Medicated Dry And Itch UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Equate Medicated Dry And 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:
- WATER (UNII: 059QF0KO0R)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X)
- GLYCERIN (UNII: PDC6A3C0OX)
- STEARAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: W6000VEI5Y)
- PETROLATUM (UNII: 4T6H12BN9U)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- STEARETH-2 (UNII: V56DFE46J5)
- STEARETH-21 (UNII: 53J3F32P58)
- .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
- EDETATE SODIUM (UNII: MP1J8420LU)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
What is the NDC to RxNorm Crosswalk for Equate Medicated Dry And Itch?
- RxCUI: 1053386 - dimethicone 5 % / menthol 0.5 % Topical Lotion
- RxCUI: 1053386 - dimethicone 50 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".