DERMAMED NATURAL HAND SANITIZER- ethanol gel

DermaMed Natural Hand Sanitizer by

Drug Labeling and Warnings

DermaMed Natural Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Biological Health Group, DermaMed Pharmaceutical Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Ethyl Alcohol 70% v/v

PURPOSE

Antimicrobial

WHEN USING

Hand sanitizer to help reduce bacteria on the skin that could cause disease
Recommended for repeated use

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.

INDICATIONS & USAGE

Place enough product in your palm to thoroughly cover your hands
Rub hands together briskly until dry
No rinsing required
No towels needed

INACTIVE INGREDIENT

Water, Aloe Vera Juice, Glycerin, Isopropyl Myristate,Tocopheryl Acetate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer,Aminomethyl Propanol, Propylene Glycol, Fragrance

KEEP OUT OF REACH OF CHILDREN

ASK DOCTOR

DOSAGE & ADMINISTRATION

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DERMAMED NATURAL HAND SANITIZER 
ethanol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69711-800
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
CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)
WATER (UNII: 059QF0KO0R)
1,2-PROPANEDITHIOL (UNII: GS64223D79)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
GLYCERIN (UNII: PDC6A3C0OX)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69711-800-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/28/2020
2	NDC: 69711-800-02	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/28/2020
3	NDC: 69711-800-03	240 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/28/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	02/28/2020

Labeler - Biological Health Group (079767886)

Establishment
Name	Address	ID/FEI	Business Operations
DermaMed Pharmaceutical Inc.		202617023	manufacture(69711-800)