Label: HANDSTAND FAS- ethyl alcohol liquid
- NDC Code(s): 79685-711-28, 79685-711-30
- 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 August 1, 2020
If you are a consumer or patient please visit this version.
- Drug Facts
- Active Ingredient
- INDICATIONS & USAGE
External use only. Flammable. Keep away from heat or flame.
Do not use
• on children less than 2 months of age
• on open skin wounds
When using this product, keep out of eyes, ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be a signs of a serious condition.
- Other Information
- INACTIVE INGREDIENT
SPL UNCLASSIFIED SECTION
Contains 70% Alcohol
Handstand FS Foaming 70% Alcohol Hand Sanitizer is highly effective against controlling microorganisms. Just rub into hands until dry. Ideal for anywhere water is not available and a high performing hand sanitizer is needed. Meets CDC recommendations for proper hand hygiene. Ideal for healthcare settings!
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.
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.
Creative Chemicals, Inc.
88 Winter St.
Holyoke, MA 01040
KEEP OUT OF REACH OF CHILDREN
For Emergencies, Call 24hr ChemTel: 800-255-3924
INGREDIENTS AND APPEARANCE
ethyl alcohol liquid
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79685-711 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 GLYCERIN (UNII: PDC6A3C0OX) HYDROGEN PEROXIDE (UNII: BBX060AN9V) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79685-711-30 300 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/30/2020 2 NDC:79685-711-28 3790 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/30/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 07/30/2020 Labeler - Creative Chemicals, Inc. (057988115) Establishment Name Address ID/FEI Business Operations Creative Chemicals, Inc. 057988115 manufacture(79685-711)