WELKIN HAND SANITIZER- alcohol gel

Welkin Hand Sanitizer by

Drug Labeling and Warnings

Welkin 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

Ethyl alcohol 70% (v/v)

Purpose

Antiseptic

Uses

• to decrease bacteria on the skin that could cause disease
• recommended for repeated use

Warnings

• For external use only
• Flammable
• Keep away from fire or flame

Do not use

• on children less than 2 months old
• on open skin wounds

When using this product

• keep out of eyes, ears, In case of contact with eyes, flush thoroughly with water.
• avoid contact with broken skin
• do not inhale or ingest

Stop use and ask a doctor if

• irritation or redness develops
• Condition persists for more than 72 hours

Keep out of reach of children.

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

Directions

• Place enough product 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

• Do not store above 105°F
• May discolor some fabrics
• Harmful to wood finishes and plastics

Inactive ingredients

aminomethyl propanol, carbomer homopolymer, glycerin, propylene glycol, purified water USP

Package Labeling:

INGREDIENTS AND APPEARANCE

WELKIN HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74979-003
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
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74979-003-01	2 mL in 1 PACKET; Type 0: Not a Combination Product	08/21/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	08/21/2020

Labeler - Robert Gordon Ind. Ltd. (070064709)