DIVINE DANDRENE 2%- zinc pyrithione shampoo 
DS Healthcare Group, Inc.

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Active ingredient

Zinc Pyrithione 2%

Purpose

Anti-dandruff

Uses

Relieves and helps prevent recurrence of scalp itch, irritation, redness, flaking and scaling associated with dandruff 

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

Directions

Apply shampoo to wet hair and scalp with gentle massage, leave in for 2-3 minutes, rinse 

For best results use atleast 2 times per week or as direacted by a doctor

For maximum benefits use 4-5 times a week along with Dandrene anti-dandruff conditioner

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

image descriptionimage descriptionimage description

DIVINE DANDRENE 2% 
zinc pyrithione shampoo
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69188-200
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC2 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69188-200-07205 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/01/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM03206/01/2021
Labeler - DS Healthcare Group, Inc. (015504134)
Establishment
NameAddressID/FEIBusiness Operations
A.I.G. Technologies, Inc086365223manufacture(69188-200)

Revised: 11/2023
Document Id: 0a477e72-d543-61d2-e063-6394a90a37e3
Set id: 54b0a610-dd15-4064-9feb-4d30b5e522ad
Version: 2
Effective Time: 20231116
 
DS Healthcare Group, Inc.