NDC 21130-424 Safeway Care Normal To Oily Hair
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 21130 - Safeway Inc
- 21130-424 - Safeway Care
Product Packages
NDC Code 21130-424-14
Package Description: 420 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 21130-424?
What are the uses for Safeway Care Normal To Oily Hair?
Which are Safeway Care Normal To Oily Hair 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 Safeway Care Normal To Oily Hair 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)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- GLYCOL DISTEARATE (UNII: 13W7MDN21W)
- ZINC CARBONATE (UNII: EQR32Y7H0M)
- MAGNESIUM SULFATE (UNII: DE08037SAB)
- SODIUM XYLENESULFONATE (UNII: G4LZF950UR)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A)
- MAGNESIUM CARBONATE HYDROXIDE (UNII: YQO029V1L4)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
What is the NDC to RxNorm Crosswalk for Safeway Care Normal To Oily Hair?
- 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".