NDC 70834-101 Md Cell Scalp
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70834 - A Joint-stock Corporation Gmc Holdings
- 70834-101 - Md Cell Scalp
Product Packages
NDC Code 70834-101-02
Package Description: 1 CONTAINER in 1 PACKAGE / 300 mL in 1 CONTAINER (70834-101-01)
Product Details
What is NDC 70834-101?
What are the uses for Md Cell Scalp?
Which are Md Cell Scalp UNII Codes?
The UNII codes for the active ingredients in this product are:
- PYRITHIONE ZINC (UNII: R953O2RHZ5)
- PYRITHIONE ZINC (UNII: R953O2RHZ5) (Active Moiety)
- PANTHENOL (UNII: WV9CM0O67Z)
- PANTHENOL (UNII: WV9CM0O67Z) (Active Moiety)
- NIACINAMIDE (UNII: 25X51I8RD4)
- NIACINAMIDE (UNII: 25X51I8RD4) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Md Cell Scalp 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-3 SULFATE (UNII: BPV390UAP0)
- AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- GLYCERIN (UNII: PDC6A3C0OX)
- POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- COCO MONOETHANOLAMIDE (UNII: C80684146D)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A)
- CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
- ZINC CHLORIDE (UNII: 86Q357L16B)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- BIOTIN (UNII: 6SO6U10H04)
- TRIDECETH-10 (UNII: G624N6MSBA)
- COCO DIETHANOLAMIDE (UNII: 92005F972D)
- SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- ARTEMISIA PRINCEPS LEAF (UNII: SY077EW02G)
- COIX LACRYMA-JOBI VAR. MA-YUEN SEED (UNII: 8DW238I7ZI)
- YEAST, UNSPECIFIED (UNII: 3NY3SM6B8U)
- NEPIDERMIN (UNII: TZK30RF92W)
- FIBROBLAST GROWTH FACTOR 7 (UNII: 9YXF283GP1)
- PREZATIDE COPPER (UNII: 6BJQ43T1I9)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
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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".