Label: HUSKY 505 ANTISEPTIC CLEANSER- chloroxylenol lotion
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Contains inactivated NDC Code(s)
NDC Code(s): 63779-505-05, 63779-505-15, 63779-505-80, 63779-505-89 - Packager: Canberra Corporation
- 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 June 28, 2010
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active Ingredient:
- Purpose:
- Uses
- Warnings
- Directions
- Other Information
- Inactive Ingredients
- Principal Display Panel
- Drum Label:
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Bag Label:
HUSKY®
505
Antiseptic Lotion Cleanser
A Powerful Antiseptic Cleanser for Handwashing
Enhanced with Moisturizers
- Reduces Bacteria on Skin That Can Potentially Cause Disease
- Assists with OSHA Bloodborne Pathogen Standard Compliance
See Drug Facts panel for additional information.
Align the half moon ears (round side out) with the
slots of the dispenser's lower docking area. Press
top and bottom of tube firmly into place.
KEEP OUT OF REACH OF CHILDREN.
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INGREDIENTS AND APPEARANCE
HUSKY 505 ANTISEPTIC CLEANSER
chloroxylenol lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63779-505 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength chloroxylenol (UNII: 0F32U78V2Q) (chloroxylenol - UNII:0F32U78V2Q) chloroxylenol 10.22 g in 1000 mL Inactive Ingredients Ingredient Name Strength water (UNII: 059QF0KO0R) potassium oleate (UNII: 74WHF607EU) cocamidopropyl betaine (UNII: 5OCF3O11KX) hydroxyethyl cellulose (2000 cps at 1%) (UNII: S38J6RZN16) isopropyl alcohol (UNII: ND2M416302) edetate sodium (UNII: MP1J8420LU) aloe vera leaf (UNII: ZY81Z83H0X) DMDM hydantoin (UNII: BYR0546TOW) triclosan (UNII: 4NM5039Y5X) potassium cocoate (UNII: F8U72V8ZXP) POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD) (UNII: 0L414VCS5Y) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63779-505-05 3785 mL in 1 BOTTLE 2 NDC:63779-505-15 208000 mL in 1 DRUM 3 NDC:63779-505-80 800 mL in 1 BAG 4 NDC:63779-505-89 490 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333 10/28/1998 Labeler - Canberra Corporation (068080621) Establishment Name Address ID/FEI Business Operations Canberra Corporation 068080621 MANUFACTURE