Active Ingredient
Zinc Pyrithione 1%
Dandrene Anti-dandruff Conditioner Lotion
FDA Label NDC 69188-300
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Ds Healthcare Group, Inc. for the product Dandrene Anti-dandruff Conditioner (NDC 69188-300). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, uses, warnings, otc - keep out of reach of children, directions, inactive ingredients, product label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
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
Otc - Keep Out Of Reach Of Children
Directions
Apply to wet hair and scalp with gentle massage, leave in for 2 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 shampoo
Inactive Ingredients
WATER, CETEARYL ALCOHOL, BEHENTRIMONIUM CHLORIDE, CETYL ESTERS, ALOE VERA GEL, KERATIN, HYDROLYZED KERATIN, AMODIMETHICONE, PEPPERMINT OIL, POLYSILICONE-15, MENTHOL, CETRIMONIUM CHLORIDE, SD ALCOHOL 40-B, DISODIUM EDTA, TRIDECETH-12, CAPRYLYL GLYCOL, METHYLISOTHIAZOLINONE
Product Label
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