NDC 76168-207 Careone Anti Itch
View Dosage, Usage, Ingredients, Routes, UNII
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Product Characteristics
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Product Details
What is NDC 76168-207?
What are the uses for Careone Anti Itch?
Which are Careone Anti Itch UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYDROCORTISONE (UNII: WI4X0X7BPJ)
- HYDROCORTISONE (UNII: WI4X0X7BPJ) (Active Moiety)
Which are Careone 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)
- OAT (UNII: Z6J799EAJK)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CHAMOMILE (UNII: FGL3685T2X)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W)
- MAGNESIUM ASCORBYL PHOSPHATE (UNII: 0R822556M5)
- MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I)
- METHYL GLUCETH-20 (UNII: J3QD0LD11P)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PETROLATUM (UNII: 4T6H12BN9U)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- WATER (UNII: 059QF0KO0R)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- STEARETH-2 (UNII: V56DFE46J5)
- STEARETH-21 (UNII: 53J3F32P58)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
What is the NDC to RxNorm Crosswalk for Careone Anti Itch?
- RxCUI: 106258 - hydrocortisone 1 % Topical Cream
- RxCUI: 106258 - hydrocortisone 10 MG/ML Topical Cream
- RxCUI: 106258 - hydrocortisone 1 % (as hydrocortisone acetate 1.2 % ) Topical Cream
- RxCUI: 106258 - hydrocortisone 1 GM per 100 GM 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".