PHYSICIANS GROUP HAND SANITIZER GEL- alcohol gel

Physicians Group Hand Sanitizer Gel by

Drug Labeling and Warnings

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

Drug Details [pdf]

Drug Facts

Active Ingredient(s)

Ethyl Alcohol 70% 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 available.

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, ear 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 contact a Poison Control Center right away.

Directions

• Place enough produt on hands to cover all surfaces. 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

Purified Water, Glycerin, H.Ethylcellulose, Trienthanolamine, Hydrogen Peroxide

Package Labeling:59ml

Package Labeling:120ml

Package Labeling:237ml

Package Labeling:473ml

Package Labeling:3.785L

INGREDIENTS AND APPEARANCE

PHYSICIANS GROUP HAND SANITIZER GEL 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77808-002
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)
ETHYLCELLULOSE, UNSPECIFIED (UNII: 7Z8S9VYZ4B)
TROLAMINE (UNII: 9O3K93S3TK)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77808-002-01	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/14/2020
2	NDC: 77808-002-02	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/14/2020
3	NDC: 77808-002-03	237 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/14/2020
4	NDC: 77808-002-04	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/14/2020
5	NDC: 77808-002-05	3785 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/14/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	07/14/2020

Labeler - Physicians Group LLC (010783019)