Label: ORCHID- triclosan liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 37808-297-08 - Packager: HEB
- Category: HUMAN OTC DRUG LABEL
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 April 13, 2012
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- ACTIVE INGREDIENT
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- WARNINGS
- DIRECTIONS
- QUESTIONS/COMMENTS?
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INACTIVE INGREDIENTS:
WATER (AQUA), SODIUM LAURETH SULFATE, ACRYLATES COPOLYMER, GLYCOL DISTEARATE, MYRISTYL ALCOHOL, COCAMIDOPROPYL BETAINE, GLYCERIN, AMMONIUM CHLORIDE, GLYCERETH-26, COCO-GLUCOSIDE, GLYCERYL OLEATE, LAURYL LACTYL LACTATE, LAVANDULA ANGUSTIFOLIA (LAVENDER) FLOWER/LEAF/STEM EXTRACT, MENTHA PIPERITA (PEPPERMINT) LEAF EXTRACT, TOCOPHERYL ACETATE, BENZOPHENONE-4, DISODIUM EDTA, SODIUM HYDROXIDE, CITRIC ACID, BENZYL ALCOHOL, FRAGRANCE (PARFUM), MANNITOL, CELLULOSE, HYDROXYPROPYL METHYLCELLULOSE, IRON OXIDES (CI 77491), EXT. VIOLET 2 (CI 60730), RED 33 (CI 17200), MICA (CI 77019), TITANIUM DIOXIDE (CI 77891), METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE.
- LABEL COPY
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INGREDIENTS AND APPEARANCE
ORCHID
triclosan liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37808-297 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 B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 1G56KV7BUJ) GLYCOL DISTEARATE (UNII: 13W7MDN21W) MYRISTYL ALCOHOL (UNII: V42034O9PU) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) GLYCERIN (UNII: PDC6A3C0OX) AMMONIUM CHLORIDE (UNII: 01Q9PC255D) GLYCERETH-26 (UNII: NNE56F2N14) COCO GLUCOSIDE (UNII: ICS790225B) GLYCERYL OLEATE (UNII: 4PC054V79P) LACTIC ACID (UNII: 33X04XA5AT) LAVANDULA ANGUSTIFOLIA FLOWERING TOP (UNII: 9YT4B71U8P) MENTHA PIPERITA LEAF (UNII: A389O33LX6) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) SULISOBENZONE (UNII: 1W6L629B4K) EDETATE DISODIUM (UNII: 7FLD91C86K) SODIUM HYDROXIDE (UNII: 55X04QC32I) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) BENZYL ALCOHOL (UNII: LKG8494WBH) MANNITOL (UNII: 3OWL53L36A) POWDERED CELLULOSE (UNII: SMD1X3XO9M) HYPROMELLOSE 2208 (4000 MPA.S) (UNII: 39J80LT57T) FERRIC OXIDE RED (UNII: 1K09F3G675) EXT. D&C VIOLET NO. 2 (UNII: G5UX3K0728) D&C RED NO. 33 (UNII: 9DBA0SBB0L) MICA (UNII: V8A1AW0880) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:37808-297-08 236 mL in 1 BOTTLE, PUMP Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 04/12/2012 Labeler - HEB (007924756) Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209) Establishment Name Address ID/FEI Business Operations APOLLO HEALTH AND BEAUTY CARE 201901209 manufacture