HAND SANITIZER- alcohol liquid

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Robert Gordon Ind. Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Alcohol 75%

Purpose

Antiseptic

Use

• For hand washing to decrease bacteria on the skin

Warnings

For External Use Only.

• Flammable, keep away from fire and flame
• Does not contain grain alcohol; do not drink.  If taken internally will produce serious gastric disturbances.

When using this product

• Avoid the eyes and mucous membranes
•  In case of eyes or mucous membranes contact, rinse area thoroughly with water

Stop use and ask a doctor if

• Condition worsens
• Redness or irritation develops
• Condition persists for more than 3 days

Keep out of reach of children.

• If swallowed, contact a doctor or Poison Control Center immediately.

Directions

• Rub dime sized amount between hands until dry.
• Supervise children in the use of this product.
• In the case of eye contact, rinse eyes thoroughly with wtaer.

​Other information

• Store below 105 oF
• May discolor some fabrics.

Inactive Ingredients

Water, Glycerin, Propylene Glycol, Fragrance, Carbomer, Aminomethyl propanol, Microcrystalline Cellulose, Lactose, Corn Starch Modified, Jojoba Esters, Ultramarines, FD&C Yellow No. 5, FD&C Blue No. 1

​Questions?

• 516-354-8888

Package Labeling: 30mL 74979-001-30

Package Labeling: 50mL 74979-001-50

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74979-001
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
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)
STARCH, CORN (UNII: O8232NY3SJ)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74979-001-30	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/20/2020
2	NDC: 74979-001-50	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/20/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/20/2020

Labeler - Robert Gordon Ind. Ltd. (070064709)