Label: ORCHID BY H E B VANILLA BROWN SUGAR- ethyl alcohol liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 37808-201-08 - Packager: H E B
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not 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 March 4, 2014
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- ACTIVE INGREDIENT
- USES
- WARNINGS
- DIRECTIONS
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INACTIVE INGREDIENTS
WATER (AQUA), SODIUM LAURETH SULFATE, ACRYLATES COPOLYER, COCAMIDOPROPYL BETAINE, CITRIC ACID, SODIU HYDROXIDE, POLYETHYLENE, SODIUM CHLORIDE, FRAGRANCE (PARFUM), PEG-7 GLYCERYL COCOATE, PROPYLENE GLYCOL, TETRASODIUM EDTA, MANNITOL, CELLULOSE, HYDROXYPROPYL METHYLCELLULOSE, CAPRYLIC/CAPRIC TRIGLYCERIDE, SODIUM STYRENE/PEG-10 MALEATE/NONOXYNOL-10 MALEATE/ACRYLATES COPOLYMER, AMMONIUM NONOXYNOL-4 SULFATE, ALOE BARBADENSIS LEAF JUICE, VANILLA PLANIFOLIA FRUIT EXTRACT, CAMELLIA SINENSIS LEAF EXTRACT, METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE, IRON OXIDES (CI 77491), IRON OXIDES (CI 77492), IRON OXIDES (CI 77499), YELLOW 5 (CI 19140), RED 33 (CI 17200), BLUE 1 (CI 42090)
- LABEL COPY
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INGREDIENTS AND APPEARANCE
ORCHID BY H E B VANILLA BROWN SUGAR
ethyl alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37808-201 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 650 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1) (UNII: 74G4R6TH13) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) SODIUM HYDROXIDE (UNII: 55X04QC32I) HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7) SODIUM CHLORIDE (UNII: 451W47IQ8X) PEG-7 GLYCERYL COCOATE (UNII: VNX7251543) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) EDETATE SODIUM (UNII: MP1J8420LU) MANNITOL (UNII: 3OWL53L36A) POWDERED CELLULOSE (UNII: SMD1X3XO9M) HYPROMELLOSES (UNII: 3NXW29V3WO) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) AMMONIUM NONOXYNOL-4 SULFATE (UNII: 9HIA70O4J0) ALOE VERA LEAF (UNII: ZY81Z83H0X) VANILLA (UNII: Q74T35078H) GREEN TEA LEAF (UNII: W2ZU1RY8B0) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) FERRIC OXIDE RED (UNII: 1K09F3G675) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) FERROSOFERRIC OXIDE (UNII: XM0M87F357) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) D&C RED NO. 33 (UNII: 9DBA0SBB0L) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:37808-201-08 236 mL in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 03/03/2014 Labeler - H E B (007924756) Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209) Establishment Name Address ID/FEI Business Operations APOLLO HEALTH AND BEAUTY CARE 201901209 manufacture(37808-201)