Label: HANDSTAND FS- benzalkonium chloride liquid
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- NDC Code(s): 79685-025-28
- Packager: Creative Chemicals, Inc.
- 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 December 19, 2021
If you are a consumer or patient please visit this version.
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- Drug Facts
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Warnings
This product is intended for external use only.
When using this product, do not use in or near the eyes. In Case of contact, rinse eyes thoroughly with water for several minutes. Remove contact lenses, if present and easy to do.
Discontinue use if irritation or redness develops. If condition persists for more than 72 hours, consult a doctor.
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- INACTIVE INGREDIENT
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SPL UNCLASSIFIED SECTION
ALCOHOL-FREE • CONTAINS 0.25% BENZALKONIUM CHLORIDE
Leaves Hands Feeling Soft
Handstand FS Foaming, Alcohol-Free Hand Sanitizer is highly effective and convenient to use anywhere soap and water are not available. Formulated with 0.25% Benzalkonium Chloride to help control microorganisms. Enhanced with humectants to moisturize skin. Pleasantly scented product does not dry skin or leave a medicinal odor like alcohol-based products. Non-flammable. Ideal where a non-alcohol product is desired.
DIRECTIONS FOR USE
Hands should be cleansed of visible soils with soap and water first. Apply small amount of product, rubbing hands thoroughly with product until dry. No rinsing needed.
KEEP OUT OF REACH OF CHILDREN
For Emergencies, call 24hr Chem Tel: 800-255-3924
Manufactured By:
Creative Chemicals, Inc.
88 Winter St.
Holyoke, MA 01040
- Packaging
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INGREDIENTS AND APPEARANCE
HANDSTAND FS
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79685-025 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.25 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79685-025-28 3790 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/30/2020 12/23/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 07/30/2020 12/23/2023 Labeler - Creative Chemicals, Inc. (057988115) Establishment Name Address ID/FEI Business Operations Creative Chemicals, Inc. 057988115 manufacture(79685-025)
