NDC 46994-511 Being Well Body Dry Scalp Care
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 46994-511?
What are the uses for Being Well Body Dry Scalp Care?
Which are Being Well Body Dry Scalp Care UNII Codes?
The UNII codes for the active ingredients in this product are:
- PYRITHIONE ZINC (UNII: R953O2RHZ5)
- PYRITHIONE ZINC (UNII: R953O2RHZ5) (Active Moiety)
Which are Being Well Body Dry Scalp Care 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:
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- COCO MONOETHANOLAMIDE (UNII: C80684146D)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- GLYCOL DISTEARATE (UNII: 13W7MDN21W)
- GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- ALMOND OIL (UNII: 66YXD4DKO9)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- TROLAMINE (UNII: 9O3K93S3TK)
- WATER (UNII: 059QF0KO0R)
- ZINC SULFATE (UNII: 89DS0H96TB)
What is the NDC to RxNorm Crosswalk for Being Well Body Dry Scalp Care?
- RxCUI: 209884 - zinc pyrithione 1 % Medicated Shampoo
- RxCUI: 209884 - zinc pyrithione 10 MG/ML Medicated Shampoo
- RxCUI: 209884 - zinc pyrithione 1 % Medicated Conditioner
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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".