Label: REXALL ALOE- selenium sulfide liquid
-
Contains inactivated NDC Code(s)
NDC Code(s): 55910-621-12 - Packager: DOLGENCORP INC
- 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 January 16, 2015
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
-
INACTIVE INGREDIENTS
WATER (AQUA), SODIUM LAURETH SULFATE, DISTEARYL PHTHALIC ACID AMIDE, SODIUM CHLRODIE, COCAMIDOPROPYL BETAINE, SODIUM STEAROYL LACTYLATE, FRAGRANCE (PARFUM), DIMETHICONE, CITRIC ACID, DMDM HYDANTOIN, SODIUM CITRATE, ALOE BARBADENSIS LEAF JUICE, HYDROXYPROPYL METHYLCELLULOSE, TITANIUM DIOXIDE, BLUE 1 (CI 42090)
- QUESTIONS OR COMMENTS?
- LABEL COPY
-
INGREDIENTS AND APPEARANCE
REXALL ALOE
selenium sulfide liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55910-621 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) DISTEARYL PHTHALAMIC ACID (UNII: 5552GSZ9LI) SODIUM CHLORIDE (UNII: 451W47IQ8X) 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) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55910-621-12 325 mL in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part358H 01/15/2015 Labeler - DOLGENCORP INC (068331990) Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209) Establishment Name Address ID/FEI Business Operations APOLLO HEALTH AND BEAUTY CARE 201901209 manufacture(55910-621)