DOCTOR SAFE- alcohol gel

DOCTOR SAFE by

Drug Labeling and Warnings

DOCTOR SAFE by is a Otc medication manufactured, distributed, or labeled by ONE DIAMOND ELECTRONICS, INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Alcohol 80% v/v

Purpose

Antiseptic

Warnings

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

Do not use:

1) in children less than 2 months of age;

2) 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. 

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

Uses

Hand Sanitizer to help reduce bacteria that potentially can cause disease.

For use when soap and water are not available.

Directions

 1) Place enough product on hands to cover all surfaces. Rub hands together until dry;

 2) Supervise children under 6 years of age when using this product to avoid swallowing.

Keep out of reach of children.

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

Other Information

1) Store between 15-30C (59-86F);

2)Avoid freezing and excessive heat above 40C (104F

Inactive Ingredient

Glycerin, Hydrogen peroxide, Purified water USP.

1.5mL

6Packs

12Packs

50packs

59mL Bottle

236mL

INGREDIENTS AND APPEARANCE

DOCTOR SAFE 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78542-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	80 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78542-001-01	1.5 mL in 1 POUCH; Type 0: Not a Combination Product	06/10/2020
2	NDC: 78542-001-02	6 in 1 BOX	06/01/2020
2		59 mL in 1 PACKAGE; Type 0: Not a Combination Product
3	NDC: 78542-001-03	12 in 1 BOX	06/01/2020
3		59 mL in 1 PACKAGE; Type 0: Not a Combination Product
4	NDC: 78542-001-04	50 in 1 BOX	06/01/2020
4		1.5 mL in 1 POUCH; Type 0: Not a Combination Product
5	NDC: 78542-001-05	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/10/2020
6	NDC: 78542-001-06	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/10/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/01/2020

Labeler - ONE DIAMOND ELECTRONICS, INC. (086508293)