BIO FORCE HAND SANITIZER 70%- alcohol gel

Bio Force Hand Sanitizer 70% by

Drug Labeling and Warnings

Bio Force Hand Sanitizer 70% by is a Otc medication manufactured, distributed, or labeled by TRASKEM SAPI de CV. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredients

Ethyl Alcohol 70% v/v

Purpose

Antiseptic

Use(s)

Hand santizer to help reduce bacteia that potentially can cause disease. For use when soap and water are not available.

Warnings

Flamable. Keep away from heat or flame. For external use only.

Do not us 

• Children less than 2 years of age.
• On open skin wounds.

When using this product

• Keep out of eyes, ears and mouth. In case of contact, rinse eyes thoroughly with water.
• Do not inhale of ingest.

Stop use and ask a doctor if 

irritation or rash occurs, these may be signs of a serious condition.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control center immediately.

Directions

• Place enough product on hands to cover all surfaces. Rub hands together until dry.
• Supervise children under 6 years of age using this product to avoid swallowing.
• Not recommended for infants.

Other inforamtion

• Store between 59-86°F (15-30°C)
• Avoid freezing and excessive heat above 104°F (40°C).
• May discolor some fanric and surfaces. Harmful to wood finishes and plastics.

Inactive Ingredients

Water, Glycerin, Isopropyl Myristate, Tocopheryl Acetate, Acrylates/C10-30 Akly Acrylate Crosspolymer

Questions?

US Domestic Telephone 832-710-8880

Package Labeling:80154-000-01

Package Labeling:80154-000-02

Package Labeling:80154-000-04

Package Labeling:80154-000-05

Package Labeling:80154-000-06

Package Labeling:80154-000-07

Bio Force Hand Sanitizer 70 %, 60 mL (TUBE) 80154-000-03

INGREDIENTS AND APPEARANCE

BIO FORCE HAND SANITIZER 70% 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80154-000
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80154-000-01	3785 mL in 1 TANK; Type 0: Not a Combination Product	07/07/2020	07/08/2020
2	NDC: 80154-000-02	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/07/2020
3	NDC: 80154-000-03	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/07/2020
4	NDC: 80154-000-04	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/07/2020
5	NDC: 80154-000-05	40 mL in 1 TUBE; Type 0: Not a Combination Product	07/07/2020
6	NDC: 80154-000-06	120 mL in 1 TUBE; Type 0: Not a Combination Product	07/07/2020
7	NDC: 80154-000-07	180 mL in 1 TUBE; Type 0: Not a Combination Product	07/07/2020
8	NDC: 80154-000-08	3785 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/07/2020
9	NDC: 80154-000-09	60 mL in 1 TUBE; Type 0: Not a Combination Product	07/07/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	07/07/2020

Labeler - TRASKEM SAPI de CV (951580813)