NDC 23637-002 Advanced Herbal Care For Thinning-damaged Hair
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 23637 - B'iota Laboratories
- 23637-002 - Advanced Herbal Care
Product Packages
NDC Code 23637-002-01
Package Description: 1 BOTTLE in 1 CARTON / 300 mL in 1 BOTTLE
Product Details
What is NDC 23637-002?
What are the uses for Advanced Herbal Care For Thinning-damaged Hair?
Which are Advanced Herbal Care For Thinning-damaged 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 Advanced Herbal Care For Thinning-damaged 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 CHLORIDE (UNII: 451W47IQ8X)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- URTICA URENS LEAF (UNII: 0DCW2P163M)
- URTICA DIOICA ROOT (UNII: J8HE8A6E5T)
- CHAMOMILE (UNII: FGL3685T2X)
- ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK)
- CAROB (UNII: 5MG5Z946UO)
- EQUISETUM ARVENSE TOP (UNII: 1DP6Y6B65Z)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- HYDROXYPROPYLTRIMONIUM CHLORIDE FRAGMENT (UNII: N30M4819DB)
- EDETATE SODIUM (UNII: MP1J8420LU)
- HONEY (UNII: Y9H1V576FH)
- C11-15 PARETH-7 (UNII: 261HPE0IS3)
- POLIDOCANOL (UNII: 0AWH8BFG9A)
- BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
- GLYCERIN (UNII: PDC6A3C0OX)
- COUMARIN (UNII: A4VZ22K1WT)
- HYDROXYISOHEXYL 3-CYCLOHEXENE CARBOXALDEHYDE (UNII: QUE43B9Z2Q)
- TRIDECETH-12 (UNII: YFY3KG5Y7O)
- VITIS VINIFERA SEED (UNII: C34U15ICXA)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
* 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".