Label: RITE AID RENEWAL- selenium sulfide liquid
-
Contains inactivated NDC Code(s)
NDC Code(s): 11822-6211-1 - Packager: RITE AID CORPORATION
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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.
Drug Label Information
Updated June 21, 2013
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- USES
- WARNINGS
- DIRECTIONS
- QUESTIONS/COMMENTS?
-
INACTIVE INGREDIENTS:
WATER (AQUA), SODIUM LAURETH SULFATE, DIHYDROGENATED TALLOW PHTHALIC ACID AMIDE, SODIUM CHLORIDE, TITANIUM DIOXIDE, COCAMIDOPROPYL BETAINE, SODIUM STEAROYL LACTYLATE, FRAGRANCE (PARFUM), DIMETHICONE, CITRIC ACID, DMDM HYDANTOIN, SODIUM CITRATE, ALOE BARBADENSIS LEAF JUICE, HYDROXYPROPYL METHYLCELLULOSE, BLUE 1 (CI 42090).
- LABEL COPY
-
INGREDIENTS AND APPEARANCE
RITE AID RENEWAL
selenium sulfide liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11822-6211 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SELENIUM SULFIDE (UNII: Z69D9E381Q) (SELENIUM SULFIDE - UNII:Z69D9E381Q) SELENIUM SULFIDE 10 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) DIHYDROGENATED TALLOW PHTHALIC ACID AMIDE (UNII: 1R81RPY10G) SODIUM CHLORIDE (UNII: 451W47IQ8X) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) SODIUM STEAROYL LACTYLATE (UNII: IN99IT31LN) DIMETHICONE (UNII: 92RU3N3Y1O) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) DMDM HYDANTOIN (UNII: BYR0546TOW) SODIUM CITRATE (UNII: 1Q73Q2JULR) ALOE VERA LEAF (UNII: ZY81Z83H0X) HYPROMELLOSES (UNII: 3NXW29V3WO) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11822-6211-1 325 mL in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part358H 06/20/2013 Labeler - RITE AID CORPORATION (014578892) Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209) Establishment Name Address ID/FEI Business Operations APOLLO HEALTH AND BEAUTY CARE 201901209 manufacture(11822-6211)