Label: FOAMFRESH ANTIBACTERIAL HAND WASH- chloroxylenol liquid
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NDC Code(s):
11429-1005-0,
11429-1005-1,
11429-1005-2,
11429-1005-3, view more11429-1005-4, 11429-1005-5, 11429-1005-6, 11429-1005-7, 11429-1005-8, 11429-1005-9
- Packager: Woodbine Products Company
- 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 June 17, 2022
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- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- STORAGE AND HANDLING
- INACTIVE INGREDIENT
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PRINCIPAL DISPLAY PANEL
FoamFresh
Antibacterial Hand Wash
The easiest way to clean
hands. A fragranced, luxuriant foam,
it is easily dispensed for an enjoyable
hand wash. Sense the difference.
Woodbine Products Company
915 West Smith Road
Medina, OH 44256
www.woodbineproducts.com
Made in USA
Stock #4510 1000 ml. (34 fl. oz.)
FoamFresh Antibacterial
Fortified with Collagen
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INGREDIENTS AND APPEARANCE
FOAMFRESH ANTIBACTERIAL HAND WASH
chloroxylenol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11429-1005 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL 2.5 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM LAURYL SULFATE (UNII: 368GB5141J) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) LAURYL GLUCOSIDE (UNII: 76LN7P7UCU) DMDM HYDANTOIN (UNII: BYR0546TOW) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11429-1005-1 59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/19/2018 2 NDC:11429-1005-2 250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/19/2018 3 NDC:11429-1005-3 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/19/2018 4 NDC:11429-1005-4 2125 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/19/2018 5 NDC:11429-1005-5 3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/19/2018 6 NDC:11429-1005-6 1500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/19/2018 7 NDC:11429-1005-7 750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/19/2018 8 NDC:11429-1005-8 1250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/19/2018 9 NDC:11429-1005-9 1100 mL in 1 BOTTLE; Type 0: Not a Combination Product 09/28/2012 10 NDC:11429-1005-0 1125 mL in 1 BOTTLE; Type 0: Not a Combination Product 09/28/2012 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 09/28/2012 Labeler - Woodbine Products Company (004220323) Establishment Name Address ID/FEI Business Operations Woodbine Products Company 004220323 manufacture(11429-1005)