Label: DELUXE ALL-PURPOSE- triclosan liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 59854-301-01 - Packager: Johnson Labs, Inc.
- 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 April 2, 2012
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Keep Out of Reach of Children
- Uses
- Warnings
- Directions
- Inactive Ingredients
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Package Label
Johnson Labs DELUXE ALL-PURPOSE LIQUID HAND SOAP
This state-of-the-art hand soap was developed to be used in industries, schools, offices or wherever people need a high quality hand soap. This product can also be used as a hair and body shampoo and clothes wash.
1 Gallon (3.78L) made in U.S.A. Johnson Labs, Inc. Troy, AL 36081 334-566-9152 800-473-9152
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INGREDIENTS AND APPEARANCE
DELUXE ALL-PURPOSE
triclosan liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59854-301 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN 7.57 mL in 3.78 L Inactive Ingredients Ingredient Name Strength SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U) COCO DIETHANOLAMIDE (UNII: 92005F972D) DMDM HYDANTOIN (UNII: BYR0546TOW) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59854-301-01 3.78 L in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 01/01/2000 Labeler - Johnson Labs, Inc. (805806742) Registrant - Johnson Labs, Inc. (805806742) Establishment Name Address ID/FEI Business Operations Johnson Labs, Inc. 805806742 manufacture