Antiseptic Foaming Hand Sanitizer
- Dosage form
- LIQUID
- Labeler
- Target Corporation
- Label updated
- 2026-02-18
- Retrieved
- 2026-09-07
- Active ingredients
- BENZALKONIUM CHLORIDE
Claims
- Made without parabens, phthalates, phenoxyethanol or sulfates**
- **Formulated without sulfated surfactants
- Not tested on animals
Active ingredient
Benzalkonium chloride 0.13%
Purpose
Antiseptic
Use
- to decrease bacteria on the skin
Warnings
For external use only – hands only
When using this product
- keep out of eyes. In case of contact with eyes, flush thoroughly with water.
- avoid contact with broken skin
Stop use and ask a doctor if
- skin irritation develops
- condition persists for more than 72 hours
Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- wet hands thoroughly with product and allow to dry without wiping
- for children under 6, use only under adult supervision
- not recommended for infants
Inactive ingredients
water, glycerin*, diglycerin, disodium cocoamphodiacetate, lauramine oxide, Aloe barbadensis leaf juice*,
sodium benzoate, cetrimonium chloride, citric acid*, methoxy PEG/PPG-7/3 aminopropyl dimethicone, propylene glycol, tetrasodium EDTA, Chamomilla recutita (matricaria) flower extract*, Pyrus malus (apple) fruit extract*, Citrus grandis (grapefruit) peel oil*, Citrus nobilis (mandarin orange) peel oil*, limonene
Claims
*Plant-derived ingredients
†Based on laboratory testing against certain bacteria
Adverse Reaction
Dist. by Target Corporation
Minneapolis, MN 55403
Made in U.S.A. with U.S. and foreign components.
TM & ©2024
Target Brands, Inc.
Guest Services
1-800-910-6874
Principal display panel
NDC 82442-812-20
Alcohol-Free
Foaming Hand Sanitizer
Citrus Scent
- Hypoallergenic
- Made with plant-derived ingredients*
- Kills 99.9% certain germs†
- Dermatologist tested
up&up ™
2-1.5 FL OZ (44 mL) TOTAL 3 FL OZ (88 mL)
[Image in the official label — see DailyMed source]
[Image in the official label — see DailyMed source]
DailyMed Set ID: 93d6e4df-9428-4557-b251-c7aa9bda3412 · Version 4
NDC: 82442-812