Label: HANDSTAND HAND SANITIZER- ethyl alcohol liquid
- NDC Code(s): 79685-701-16, 79685-701-28, 79685-701-32
- 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.
Updated December 19, 2021
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- Drug Facts
- Active Ingredient
- INDICATIONS & USAGE
Flammable. Keep away from fire or flame.
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.
Discontinue use if irritation or redness develops. If condition persists for more than 72 hours, consult a doctor.
- Other Information
- INACTIVE INGREDIENT
SPL UNCLASSIFIED SECTION
CONTAINS 70% ETHYL ALCOHOL
ALCOHOL ANTISEPTIC TOPICAL • LEAVES HANDS FELLING SOFT
DIRECTIONS FOR USE
Place enough product in your palm to thoroughly cover your hands. Rub hands together briskly until dry. Children under 6 years of age should be supervised when using this product. Store between 15-30 C (59-86 F). May discolor certain fabrics or surfaces.
Warnings. Flammable. Keep away from fire or flame. 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. Stop use and ask a doctor if irritation or rash appears and lasts. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
KEEP OUT OF REACH OF CHILDREN
For Emergencies, Call 24hr ChemTel: 800-255-3924
Creative Chemicals, Inc.
88 Winter St.
Holyoke, MA 01040
INGREDIENTS AND APPEARANCE
HANDSTAND HAND SANITIZER
ethyl alcohol liquid
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79685-701 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) (UNII: S38J6RZN16) GLYCERIN (UNII: PDC6A3C0OX) HYDROGEN PEROXIDE (UNII: BBX060AN9V) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79685-701-16 473 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/30/2020 12/23/2023 2 NDC:79685-701-32 950 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/30/2020 12/23/2023 3 NDC:79685-701-28 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(79685-701)