Label: DIVINE DANDRENE 1%- zinc pyrithione shampoo
- NDC Code(s): 69188-100-07
- Packager: DS Healthcare Group, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 8, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
-
Warnings
For external use only.
When using this Product: Avoid contact with eyes, If contact occurs, rinse eyes thoroughly with water
Stop use and ask a doctor if Condition worsens or does not improve after regular use of this product as directed
Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away
- KEEP OUT OF REACH OF CHILDREN
- Directions
-
Inactive ingredients
Water, Disodium Laureth Sulfosuccinate, Triethanolamine, Glycolic Acid, Cocamide MEA, Sodium Lauroyl Sarcosinate, Sodium Lauryl Suloacetate, Glycol Distearate, PEG-150 Distearate, Magnesium Aluminum Silicate, Sodium Citrate, Hexamidine Diisethionate, Hydrolyzed Lupine
Protein, Caprylyl Glycol, Phenoxyethanol, Butylene Glycol, Punica Granatum Extract, Rosmarinus Officinalis Leaf Extract, Shikimic Acid, Tioxolone, Blue 1 - Product label
-
INGREDIENTS AND APPEARANCE
DIVINE DANDRENE 1%
zinc pyrithione shampooProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69188-100 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 WATER (UNII: 059QF0KO0R) DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E) TROLAMINE (UNII: 9O3K93S3TK) GLYCOLIC ACID (UNII: 0WT12SX38S) COCO MONOETHANOLAMIDE (UNII: C80684146D) SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618) SODIUM LAURYL SULFOACETATE (UNII: D0Y70F2B9J) GLYCOL DISTEARATE (UNII: 13W7MDN21W) PEG-150 DISTEARATE (UNII: 6F36Q0I0AC) MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC) SODIUM CITRATE (UNII: 1Q73Q2JULR) HEXAMIDINE DIISETHIONATE (UNII: 023XA5Z50L) SURINAMINE (UNII: AIQ58N56TM) CAPRYLYL GLYCOL (UNII: 00YIU5438U) PHENOXYETHANOL (UNII: HIE492ZZ3T) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) PUNICA GRANATUM FLOWER (UNII: D9B634V4GP) ROSEMARY (UNII: IJ67X351P9) SHIKIMIC ACID (UNII: 29MS2WI2NU) TIOXOLONE (UNII: S0FAJ1R9CD) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69188-100-07 205 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/01/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M032 06/01/2021 Labeler - DS Healthcare Group, Inc. (015504134) Establishment Name Address ID/FEI Business Operations A.I.G. Technologies, Inc 086365223 manufacture(69188-100)