Label: BETADINE FOAM CLEANSER- benzalkonium chloride aerosol, foam
- NDC Code(s): 67618-184-08
- Packager: Atlantis Consumer Healthcare, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 5, 2025
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- Official Label (Printer Friendly)
- Drug Facts
- Purpose
- Uses
- Warnings
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children.
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- Other information
- Inactive ingredients
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Package Labels
BETADINE®
HAND & SKIN
CLEANSER
Antimicrobial
Foam Skin Cleanser
Hospital Grade,
Broad Spectrum
Germ Killing*
Great for Hand
& Skin Hygiene
Skin Softening
Formula
with Aloe
HAND WASHING
GENERAL SKIN CLEANSING
8 fl oz (237 mL)
BETADINE®
HAND & SKIN CLEANSER
*Based on in vitro lab testing
Dist. by: Atlantis Consumer Healthcare Inc., Bridgewater, NJ 08807 USA
Betadine is a registered trademark of Atlantis Consumer Healthcare Inc
© 2025 Atlantis Healthcare Inc. A0925
BETADINE®
HAND & SKIN
CLEANSER
Antimicrobial Foam
Skin Cleanser
NEW!
Hospital Grade,
Broad Spectrum
Germ Killing*
Kills 99.9% of 20
Different Bacteria
in Seconds*
Great for Hand
& Skin Hygiene
Skin Softening
Formula
with Aloe
HAND WASHING
GENERAL SKIN CLEANSING
8 fl oz (237 mL)
Distributed by:
Atlantis Consumer Healthcare Inc., Bridgewater, NJ 08807 USA
Betadine is a registered trademark of Atlantis Consumer
Healthcare Inc.
© 2025 Atlantis Health Care Inc.
*Based on in vitro lab testing
A0925
-
INGREDIENTS AND APPEARANCE
BETADINE FOAM CLEANSER
benzalkonium chloride aerosol, foamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:67618-184 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Benzalkonium Chloride (UNII: F5UM2KM3W7) (Benzalkonium - UNII:7N6JUD5X6Y) Benzalkonium Chloride 0.13 g in 100 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Glycerin (UNII: PDC6A3C0OX) Cocamidopropyl Betaine (UNII: 5OCF3O11KX) Lauramine Oxide (UNII: 4F6FC4MI8W) Phenoxyethanol (UNII: HIE492ZZ3T) Coco Monoethanolamide (UNII: C80684146D) Edetate Sodium (UNII: MP1J8420LU) Peg-150 Distearate (UNII: 6F36Q0I0AC) Aloe Vera Leaf Juice (UNII: RUE8E6T4NB) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:67618-184-08 237 mL in 1 BOTTLE; Type 0: Not a Combination Product 02/01/2026 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M003 02/01/2026 Labeler - Atlantis Consumer Healthcare, Inc. (118983925)
