HUSKY 505 ANTISEPTIC CLEANSER- chloroxylenol lotion 
Canberra Corporation

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.

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Antiseptic Lotion Cleanser

Drug Facts

Active Ingredient:

Chloroxylenol (1% v/v)

Purpose:

Antiseptic Hand Sanitizer

Uses

Warnings

Directions

Other Information

Inactive Ingredients

Water, Cocoate, Oleate, Cocamidopropyl betaine, Hydroxyethyl Cellulose, Polyquaternium 7, Na4EDTA, 2-Propanol, Peg-75 Lanolin, Aloe Vera Gel, Fragrance, Triclosan, DMDM Hydantoin.

Principal Display Panel

Bottle Label:

HUSKY®

505

Antiseptic Lotion Cleanser

A Powerful Antiseptic Cleanser for Handwashing

Enhanced with Moisturizers

See Drug Facts panel for additional information.

Bottle Label

Drum Label:

HUSKY®

505

Antiseptic Lotion Cleanser

A Powerful Antiseptic Cleanser for Handwashing

Enhanced with Moisturizers

See Drug Facts panel for additional information.

Drum Label

Bag Label:

HUSKY®

505

Antiseptic Lotion Cleanser

A Powerful Antiseptic Cleanser for Handwashing

Enhanced with Moisturizers

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.

Bag Label
HUSKY 505 ANTISEPTIC CLEANSER 
chloroxylenol lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63779-505
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
chloroxylenol (UNII: 0F32U78V2Q) (chloroxylenol - UNII:0F32U78V2Q) chloroxylenol10.22 g  in 1000 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63779-505-053785 mL in 1 BOTTLE
2NDC:63779-505-15208000 mL in 1 DRUM
3NDC:63779-505-80800 mL in 1 BAG
4NDC:63779-505-89490 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33310/28/1998
Labeler - Canberra Corporation (068080621)
Establishment
NameAddressID/FEIBusiness Operations
Canberra Corporation068080621MANUFACTURE

Revised: 6/2010
Document Id: 369a14d0-8977-471f-9e09-6b07a0e49a8c
Set id: 1e285837-a620-44c2-80f0-589a9b847edb
Version: 1
Effective Time: 20100628
 
Canberra Corporation