CAREONE MEDICATED DANDRUFF- selenium sulfide liquid
AMERICAN SALES COMPANY
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.
----------
FOR THE RELIEF OF FLAKING AND ITCHING ASSOCIATED WITH DANDRUFF AND SEBORRHEIC DERMATITIS AND TO HELP PREVENT THE CHANCE OF RECURRENCE
FOR EXTERNAL USE ONLY
SHAKE WELL, APPLY SHAMPOO AND RINSE THOROUGHLY. FOR BEST RESULTS, USE AT LEAST TWICE A WEEK OR AS DIRECTED BY A DOCTOR
WATER (AQUA), SODIUM LAURETH SULFATE, TEA-LAURYL SULFATE, COCAMIDOPROPYL BETAINE, ACRYLATES COPOLYMER, CITRIC ACID, AMMONIUM CHLORIDE, SODIUM HYDROXIDE, DMDM HYDANTOIN, FRAGRANCE (PARFUM), MAGNESIUM ALUMINUM SILICATE, HYDROXYPROPYL METHYLCELLULOSE, MENTHOL, BLUE 1 (CI 42090), RED 33 (CI 17200)
CAREONE
MEDICATED DANDRUFF
selenium sulfide liquid |
||||||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||||||
|
Labeler - AMERICAN SALES COMPANY (809183973) |
Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209) |
Establishment | |||
Name | Address | ID/FEI | Business Operations |
---|---|---|---|
APOLLO HEALTH AND BEAUTY CARE | 201901209 | manufacture(41520-719) |