Label: ANTISEPTIC SKIN CLEANSER- chlorhexidine gluconate 4% liquid
- NDC Code(s): 0363-1061-08, 0363-1061-15, 0363-1061-16, 0363-1061-18
- Packager: Walgreen Co.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated November 8, 2024
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
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Warnings
For external use only
Allergy alert:
This product may cause a severe allergic reaction. Sypmtoms may include:
- wheezing/difficulty breathing
- shock
- facial swelling
- hives
- rash
If an allergic reaction occurs, stop use and seek medical help right away.
Do not use
- if you of the patient is allergic to chlorhexidine gluconate or any other ingredient in this product
- in contact with meninges
- in the genital area
When using this product
- keep out of eyes, ears, and mouth. May cause serious and permanent eye injury if permitted to enter and remain in the eye or may cause deafness when instilled in the middle ear through perforated eardrums.
- if solution should contact these areas, rinse out promptly and thoroughly with water
- wounds which involve more than the superficial layers of the skin should not be routinely treated
- repeated general skin cleansing of large body areas should not be done except when advised by a health care provider
- Uses
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Directions
- use with care in premature infants or infants under 2 months of age. These products may cause irritation or chemical burns.
Healthcare personnel handwash:
- wet hands with water
- dispense about 5 mL of product into cupped hands and wash in a vigorous manner for about 15 seconds
- rinse and dry thoroughly
Skin wound and normal skin cleansing:
- thoroughly rinse the area to be cleaned with water
- apply the minimum amount of product necessary to cover the skin or wound area and wash gently
- rinse again thoroughly
- Other information
- Inactive ingredients
- Questions or comments?
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OTHER SAFETY INFORMATION
Laundering/Cleaning Instructions: Chlorhexidine gluconate skin cleansers will cause stains if used with chlorine-releasing products, such as chlorine bleach. Rinse completely and use only non-chlorine detergents.
WARNING: This product contains a chemical (cocamide DEA) known to the State of California to cause cancer.
‡Walgreens Pharmacist Survey Study, November 2014
‡‡This product is not manufactured or distributed by Mölnlycke Healthcare, owner of the registered trademark Hibiclens®.
Distributed by: Walgreen Co.
200 Wilmot RD., Deerfield, IL 60015
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©2015 Walgreen Co. Made in USA
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Package label and principal display panel
Walgreens
Dye-Free
Antiseptic Skin Cleanser
Chlorhexidine Gluconate 4% Solution/Antiseptic/Antimicrobial Skin Cleanser
Compare to the active ingredient in Hibiclens®‡
8 FL OZ. (237 mL)
TAMPER EVIDENT: DO NOT USE IF SAFETY SEAL IS BROKEN OR MISSING.
4WA08BTLLBLH
NDC 0363-1061-08
Walgreens
Dye Free
Antiseptic Skin Cleanser
Chlorhexidine Gluconate 4% Solution/Antiseptic/Antimicrobial Skin Cleanser
Compare to the active ingredient in Hibiclens®‡
16 FL OZ. (473 mL)
TAMPER EVIDENT: DO NOT USE IF SAFETY SEAL IS BROKEN OR MISSING.
4WA16BTLLBLE
NDC 0363-1061-16
Walgreens
Dye-Free
Antiseptic Foaming Skin Cleanser
CHLORHEXIDINE GLUCONATE 4% SOLUTION /
ANTISEPTIC / ANTIMICROBIAL SKIN CLEANSER
Compare to Hibiclens® active ingredient
18 FL OZ (532 mL)
NDC 0363-1061-184WA18FM1061LBLB
- Carton
- Lidstock
- Packet
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INGREDIENTS AND APPEARANCE
ANTISEPTIC SKIN CLEANSER
chlorhexidine gluconate 4% liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-1061 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) (CHLORHEXIDINE - UNII:R4KO0DY52L) CHLORHEXIDINE GLUCONATE 4 mg in 100 mL Inactive Ingredients Ingredient Name Strength LAURAMINE OXIDE (UNII: 4F6FC4MI8W) COCO DIETHANOLAMIDE (UNII: 92005F972D) PEG-75 LANOLIN (UNII: 09179OX7TB) HYDROXYETHYL CELLULOSE (2000 CPS AT 1%) (UNII: S38J6RZN16) ISOPROPYL ALCOHOL (UNII: ND2M416302) WATER (UNII: 059QF0KO0R) TRIDECYL ALCOHOL (UNII: 8I9428H868) GLUCONOLACTONE (UNII: WQ29KQ9POT) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-1061-08 237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/01/2011 2 NDC:0363-1061-16 473 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/01/2011 3 NDC:0363-1061-15 15 mL in 1 KIT; Type 1: Convenience Kit of Co-Package 01/01/2017 4 NDC:0363-1061-18 532 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 01/11/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA019125 05/01/2011 Labeler - Walgreen Co. (008965063) Registrant - Xttrium Laboratories, Inc. (007470579) Establishment Name Address ID/FEI Business Operations Xttrium Laboratories, Inc. 007470579 manufacture(0363-1061)
