NDC 13537-751 Esika Men 2 En 1 Antidandruff Multi-action
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 13537 - Ventura Corporation Ltd
- 13537-751 - Esika Men 2 En 1 Antidandruff Multi-action
Product Packages
NDC Code 13537-751-01
Package Description: 300 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 13537-751?
What are the uses for Esika Men 2 En 1 Antidandruff Multi-action?
Which are Esika Men 2 En 1 Antidandruff Multi-action 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 Esika Men 2 En 1 Antidandruff Multi-action 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)
- COCO DIETHANOLAMIDE (UNII: 92005F972D)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- HYDROLYZED SOY PROTEIN (ENZYMATIC; 2000 MW) (UNII: 1394NXB9L6)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- GLYCOL DISTEARATE (UNII: 13W7MDN21W)
- TROLAMINE (UNII: 9O3K93S3TK)
- GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A)
- COCO GLUCOSIDE (UNII: ICS790225B)
- TRIETHANOLAMINE DODECYLBENZENESULFONATE (UNII: 8HM7ZD48HN)
- HYDROLYZED WHEAT PROTEIN (ENZYMATIC; 3000 MW) (UNII: J2S07SB0YL)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- GLYCERYL OLEATE (UNII: 4PC054V79P)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- MAGNESIUM NITRATE (UNII: 77CBG3UN78)
- ZINC CHLORIDE (UNII: 86Q357L16B)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- BAMBUSA BAMBOS LEAF (UNII: HW86D1FGSS)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- PANTHENOL (UNII: WV9CM0O67Z)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
- PPG-26-BUTETH-26 (UNII: 2II1K6TZ4P)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- MENTHYL DL-PYRROLIDONECARBOXYLATE (UNII: 8P18J856U2)
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- APIGENIN (UNII: 7V515PI7F6)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
- OLEANOLIC ACID (UNII: 6SMK8R7TGJ)
- BIOTINOYL TRIPEPTIDE-1 (UNII: O6380721VA)
- .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
- .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
* 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".