Label: JASMINE TEA AND BASIL ANTIBACTERIAL HAND SP- triclosan liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 37808-290-08 - Packager: HEB
- 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 December 23, 2010
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- ACTIVE INGREDIENT
- PURPOSE
- USES
- WARNINGS
- DIRECTIONS
- QUESTIONS OR COMMENTS
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INACTIVE INGREDIENTS
WATER, SODIUM LAURETH SULFATE, ACRYLATES COPOLYMER, COCAMIDOPROPYL BETAINE, COCAMIDE DEA, SODIUM CHLORIDE, FRAGRANCE (PARFUM), ALOE BARBADENSIS LEAF JUICE, PEG-7 GLYCERYL COCOATE, HELIANTHUS ANNUUS (SUNFLOWER) EXTRACT, JASMINUM OFFICINALE (JASMINE) FLOWER/LEAF EXTRACT, CAMELLIA SINENSIS LEAF EXTRACT, OCIMUM BASILICUM (BASIL) FLOWER/LEAF EXTRACT, TETRASODIUM EDTA, SODIUM STYRENE/PEG-10 MALEATE/NONOXYNOL-10 MALEATE/ACRYLATES COPOLYMER, AMMONIUM NONOXYNOL-4 SULFATE, CITRIC ACID, SODIUM HYDROXIDE, MANNITOL, CELLULOSE, HYDROXYPROPYL METHYLCELLULOSE, MICA, TITANIUM OXIDE (CI 77891), CHROMIUM HYDROXIDE GREEN (CI 77289), YELLOW 5 (CI 19140), BLUE 1 (CI 42090), METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE.
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
JASMINE TEA AND BASIL ANTIBACTERIAL HAND SP
triclosan liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37808-290 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN 0.3 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) COCO DIETHANOLAMIDE (UNII: 92005F972D) SODIUM CHLORIDE (UNII: 451W47IQ8X) ALOE VERA LEAF (UNII: ZY81Z83H0X) GLYCERYL COCOATE (UNII: WVK1CT5994) SUNFLOWER SEED (UNII: R9N3379M4Z) JASMINUM OFFICINALE FLOWER (UNII: 0Q8K841432) GREEN TEA LEAF (UNII: W2ZU1RY8B0) BASIL (UNII: 2U0KZP0FDW) LOW DENSITY POLYETHYLENE (UNII: J245LN42AI) EDETATE SODIUM (UNII: MP1J8420LU) NONOXYNOL-10 (UNII: K7O76887AP) AMMONIUM NONOXYNOL-4 SULFATE (UNII: 9HIA70O4J0) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) SODIUM HYDROXIDE (UNII: 55X04QC32I) MANNITOL (UNII: 3OWL53L36A) CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) HYPROMELLOSES (UNII: 3NXW29V3WO) MICA (UNII: V8A1AW0880) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) CHROMIC OXIDE (UNII: X5Z09SU859) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:37808-290-08 236 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 12/30/2010 Labeler - HEB (007924756) Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209) Establishment Name Address ID/FEI Business Operations APOLLO HEALTH AND BEAUTY CARE 201901209 manufacture