Label: ANTIBACTERIAL SUNBLOSSOM- triclosan soap
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Contains inactivated NDC Code(s)
NDC Code(s): 59779-284-09 - Packager: CVS Pharmacy
- 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 24, 2010
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- Active Ingredient
- Purpose
- Warnings
- Uses
- Directions
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Inactive Ingredients
Water (Aqua), Sodium Laureth Sulfate, Acrylates Copolymer, Cocamidopropyl Betaine, Cocamide DEA, Sodium Chloride, Fragrance (Parfum), Aloe Barbadensis Leaf Juice, PEG-7 Glyceryl Cocoate, Helianthus Annuus (Sunflower) Seed Extract, Tetrasodium EDTA, Sodium Styrene/PEG-10 Maleate/Nonoxynol-10 Maleate/ Acrylates Copolymer, Ammonium Nonoxynol-4 Sulfate, Citric Acid, Sodium Hydroxide, Mannitol, Cellulose, Tocopheryl Acetate, Hydroxypropyl Methylcellulose, Mica, Titanium Oxide (CI 77891), Yellow 10 (CI 47005), Red 40 (CI 16035), Iron Oxides ( CI 77492), Methylchloroisothiazolinone, Methylisothiazolinone.
- PACKAGE FRONT AND BACK LABELS
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INGREDIENTS AND APPEARANCE
ANTIBACTERIAL SUNBLOSSOM
triclosan soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59779-284 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN 0.3000 mL in 100.0000 mL Product Characteristics Color orange Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59779-284-09 251.00 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 08/24/2010 Labeler - CVS Pharmacy (062312574)