Label: ORCHID JASMINE TEA AND BASIL- triclosan liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 37808-090-08 - 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 August 13, 2013
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- ACTIVE INGREDIENT
- USES
- WARNINGS
- DIRECTIONS
- QUESTIONS/COMMENTS?
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INACTIVE INGREDIENTS:
WATER (AQUA), SODIUM LAURETH SULFATE, ACRYLATES COPOLYMER, COCAMIDOPROPYL BETAINE, FRAGRANCE (pARFUM), SODIUM CHLORIDE, CITRIC ACID, POLYETHYLENE, SODIUM HYDROXIDE, PEG-7 GLYCERYL COCOATE, PROPYLENE GLYCOL, TETRASODIUM EDTA, MANNITOL, CELLULOSE, HYDROXYPROPYL METHYLCELLULOSE, TOCOPHERYL ACETATE, SODIUM STYRENE/PEG-10 MALEATE/NONOXYNOL-10 MALEATE/ACRYLATES COPOLYMER, AMMONIUM NONOXYNOL-4 SULFATE, ALOE BARBADENSIS LEAF JUICE POWDER, HELIANTHUS ANNUUS (SUNFLOWER) EXTRACT, JASMINUM OFFICINALE (JASMINE) FLOWER/LEAF EXTRACT, CAMELLIA SINENSIS LEAF EXTRACT, OCIMUM BASILICUM (BASIL) FLOWER/LEAF EXTRACT, METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE, CHROMIUM HYDROXIDE GREEN (CI 77289), YELLOW 5 (CI 19140), BLUE 1 (CI 42090).
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INGREDIENTS AND APPEARANCE
ORCHID JASMINE TEA AND BASIL
triclosan liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37808-090 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN 3 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) SODIUM CHLORIDE (UNII: 451W47IQ8X) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7) SODIUM HYDROXIDE (UNII: 55X04QC32I) PEG-7 GLYCERYL COCOATE (UNII: VNX7251543) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) EDETATE SODIUM (UNII: MP1J8420LU) MANNITOL (UNII: 3OWL53L36A) POWDERED CELLULOSE (UNII: SMD1X3XO9M) HYPROMELLOSES (UNII: 3NXW29V3WO) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) AMMONIUM NONOXYNOL-4 SULFATE (UNII: 9HIA70O4J0) ALOE VERA LEAF (UNII: ZY81Z83H0X) HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP) JASMINUM OFFICINALE FLOWER (UNII: 0Q8K841432) GREEN TEA LEAF (UNII: W2ZU1RY8B0) OCIMUM BASILICUM FLOWERING TOP (UNII: 7SAB275FP2) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) CHROMIUM HYDROXIDE GREEN (UNII: RV8FT8XF5R) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:37808-090-08 236 mL in 1 BOTTLE, PLASTIC 08/12/2013 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 08/12/2013 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(37808-090)
