PHYSICIANS GROUP HAND SANITIZER- alcohol liquid

Physicians Group Hand Sanitizer by

Drug Labeling and Warnings

Physicians Group Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Physicians Group, L.L.C.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient(s)

Ethyl Alcohol 75% v/v

Purpose

Antiseptic

Use(s)

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not availble.

Warnings

For 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 signs of a serious condition.

KEEP OUT OF REACH OF CHILDREN.

If swallowed, get medical help or contact a Poison Contol Center right away.

Directions

• Place enough product on hands to cover all surface. Rub hands together until dry.
• Supervise children under 6 years of age when using this product to avoid swallowing.

Other Information

• Store between 15-30°C(59-86°F)
• Avoid freezing and excessive heat above 40°C(104°F)

Inactive Ingredients

glycerin, hydrogen peroxide, purified water USP

Package Labeling : 59ml

Package Labeling: 120ml

Package Labeling: 237ml

Package Labeling: 473ml

Package Labeling: 3785ml

INGREDIENTS AND APPEARANCE

PHYSICIANS GROUP HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77808-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.75 mL  in 1 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: 77808-001-01	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/15/2020
2	NDC: 77808-001-02	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/15/2020
3	NDC: 77808-001-03	237 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/15/2020
4	NDC: 77808-001-04	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/15/2020
5	NDC: 77808-001-05	3785 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/15/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/15/2020

Labeler - Physicians Group LLC- 4054 Sawyer (010783019)