Label: ORCHID BY H E B VANILLA BROWN SUGAR- triclosan liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 37808-107-08 - 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
- QUESTIONS/COMMENTS?
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INACTIVE INGREDIENTS
WATER (AQUA), SODIUM LAURETH SULFATE, COCAMIDOPROPYLAMINE OXIDE, DISODIUM LAURETH SULFOSUCCINATE, PPG-1-PEG-9 LAURYL GLYCOL ETHER, FRAGRANCE (PARFUM), PEG-7 GLYCERYL COCOATE, GLYCERIN, TETRASODIUM EDTA, BENZOPHENONE-4, BENZYL ALCOHOL, SODIUM CHLORIDE, GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE, PROPYLENE GLYCOL, HYDROXYPROPYL METHYLCELLULOSE, ALOE BARBADENSIS LEAF JUICE, VANILLA PLANIFOLIA FRUIT EXTRACT, CAMELLIA SINENSIS LEAF EXTRACT, CITRIC ACID, SODIUM HYDROXIDE, METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE, 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
triclosan liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37808-107 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN 4.6 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK) DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E) PPG-1-PEG-9 LAURYL GLYCOL ETHER (UNII: 5R8J43K25L) PEG-7 GLYCERYL COCOATE (UNII: VNX7251543) GLYCERIN (UNII: PDC6A3C0OX) EDETATE SODIUM (UNII: MP1J8420LU) SULIBENZONE (UNII: 853Z42ZYAS) BENZYL ALCOHOL (UNII: LKG8494WBH) SODIUM CHLORIDE (UNII: 451W47IQ8X) GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) HYPROMELLOSES (UNII: 3NXW29V3WO) ALOE VERA LEAF (UNII: ZY81Z83H0X) VANILLA (UNII: Q74T35078H) GREEN TEA LEAF (UNII: W2ZU1RY8B0) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) SODIUM HYDROXIDE (UNII: 55X04QC32I) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) 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:37808-107-08 236 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(37808-107)