NDC 69423-569 Head And Shoulders Supreme Scalp Moisturizer With Hemp Seed
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69423 - The Procter & Gamble Manufacturing Company
- 69423-569 - Head And Shoulders Supreme Scalp Moisturizer With Hemp Seed
Product Packages
NDC Code 69423-569-50
Package Description: 50 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 69423-569?
What are the uses for Head And Shoulders Supreme Scalp Moisturizer With Hemp Seed?
Which are Head And Shoulders Supreme Scalp Moisturizer With Hemp Seed 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 Head And Shoulders Supreme Scalp Moisturizer With Hemp Seed 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:
- STEARAMIDOPROPYL DIMETHYLAMINE (UNII: K7VEI00UFR)
- HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYETHYLENE OXIDE 100000 (UNII: V46Y6OJ5QB)
- OLEYL ALCOHOL (UNII: 172F2WN8DV)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- QUATERNIUM-18 (UNII: O7757NO1VL)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- WATER (UNII: 059QF0KO0R)
- CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- DIMETHICONE (UNII: 92RU3N3Y1O)
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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".