Label: LEUDINE ANTI-DANDRUFF- pyrithione zinc shampoo
-
Contains inactivated NDC Code(s)
NDC Code(s): 76482-013-02 - Packager: B&R Products Inc
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated February 13, 2013
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Keep Out of Reach of Children
- Uses
- Warnings
- Directions
-
Inactive ingredients
Acrylates Copolymer, Ammonium Laureth Sulfate, Ammonium Lauryl Sulfate, Ammonium Xylenesulfonate, Citric Acid, Cocamide MEA, Cocamidopropyl PG-Dimonium Chloride, Fragrance, Glycol Distearate, Guar Hydroxypropyltrimonium Chloride, Methylchloroisothiazolinone, Methylisothiazolinone, Panthenol, Sodium Chloride, Triethanolamine, Water, Blue 1.
- Questions?
- Package/Label Principal Display Panel
-
INGREDIENTS AND APPEARANCE
LEUDINE ANTI-DANDRUFF
pyrithione zinc shampooProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76482-013 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC 1 g in 100 mL Inactive Ingredients Ingredient Name Strength ETHYL ACRYLATE AND METHYL METHACRYLATE COPOLYMER (2:1; 600000 MW) (UNII: XRK36F13ZZ) AMMONIUM LAURETH-2 SULFATE (UNII: 698O4Z48G6) AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B) AMMONIUM XYLENESULFONATE (UNII: 4FZY6L6XCM) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) COCO MONOETHANOLAMIDE (UNII: C80684146D) COCAMIDOPROPYL PG-DIMONIUM CHLORIDE (UNII: 205Z54J075) GLYCOL DISTEARATE (UNII: 13W7MDN21W) GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) PANTHENOL (UNII: WV9CM0O67Z) SODIUM CHLORIDE (UNII: 451W47IQ8X) TROLAMINE (UNII: 9O3K93S3TK) WATER (UNII: 059QF0KO0R) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76482-013-02 60 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part358H 04/01/2013 Labeler - B&R Products Inc (085560514) Registrant - B&R Products Inc (085560514) Establishment Name Address ID/FEI Business Operations B&R Products Inc 085560514 MANUFACTURE(76482-013)