Your browser does not support JavaScript! RITE AID RENEWAL MEDICATED (SELENIUM SULFIDE) LIQUID [RITE AID CORPORATION]
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RITE AID RENEWAL MEDICATED (selenium sulfide) liquid
[RITE AID CORPORATION]


Category DEA Schedule Marketing Status
HUMAN OTC DRUG LABEL OTC monograph final
NOTE: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 Sections

ACTIVE INGREDIENT

SELENIUM SULFIDE 1%

PURPOSE

ANTI-DANDRUFF, ANTI-SEBORREIC DERMATITIS

USES

FOR RELIEF OF FLAKING AND ITCHING DUE TO DANDRUFF, AND SEBORRHEIC DERMATITIS, AND TO HELP PREVENT THE CHANCE OF RECURRENCE.

WARNINGS

FOR EXTERNAL USE ONLY.

ASK A DOCTOR BEFORE USING IF YOU HAVE

SEBORRHEIC DERMATITIS IN AREAS OTHER THAN THE SCALP.

WHEN USING THIS PRODUCT

AVOID CONTACT WITH THE EYES. IF CONTACT OCCURS, RINSE EYES THOROUGHLY WITH WATER. FOR USE ON COLOR-TREATED OR PERMED HAIR, RINSE THOROUGHLY.

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 A POISON CONTROL CENTER RIGHT AWAY.

DIRECTIONS

SHAKE WELL. SHAMPOO, THEN RINSE THOROUGHLY. FOR BEST RESULTS, USE AT LEAST TWICE A WEEK OR AS DIRECTED BY A DOCTOR.

QUESTIONS/COMMENTS?

1-866-695-3030

INACTIVE INGREDIENTS:

WATER (AQUA), SODIUM LAURETH SULFATE, ACRYLATES COPOLYMER, TEA-LAURETH SULFATE, COCAMIDOPROPYL BETAINE, CITRIC ACID, AMMONIUM CHLORIDE, FRAGRANCE (PARFUM), DMDM HYDANTOIN, SODIUM HYDROXIDE, MENTHOL, MAGNESIUM ALUMINUM SILICATE, HYDROXYPROPYL METHYLCELLULOSE, BLUE 1 (CI 42090), RED 33 (CI 17200).

LABEL COPY

IMAGE OF THE LABEL

RITE AID RENEWAL  MEDICATED
selenium sulfide liquid
Product Information
Product TypeHUMAN OTC DRUG LABELItem Code (Source)NDC:11822-6201
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SELENIUM SULFIDE (SELENIUM SULFIDE) SELENIUM SULFIDE10 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
SODIUM LAURETH SULFATE 
METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1) 
TRIETHANOLAMINE LAURYL SULFATE 
COCAMIDOPROPYL BETAINE 
CITRIC ACID MONOHYDRATE 
AMMONIUM CHLORIDE 
DMDM HYDANTOIN 
SODIUM HYDROXIDE 
MENTHOL 
MAGNESIUM ALUMINUM SILICATE 
HYPROMELLOSES 
FD&C BLUE NO. 1 
D&C RED NO. 33 
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11822-6201-1325 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358H07/15/2013
Labeler - RITE AID CORPORATION (014578892)
Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209)
Establishment
NameAddressID/FEIBusiness Operations
APOLLO HEALTH AND BEAUTY CARE201901209manufacture(11822-6201)

Revised: 7/2013
 
RITE AID CORPORATION

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