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 Ningbo SKL International Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl alcohol 70% (v/v)

Purpose

Antiseptic

Use

• 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, 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

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 USPglycerin, hydrogen peroxide, purified water USP

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

WELKIN HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74542-014
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
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
CARBOMER HOMOPOLYMER TYPE A (UNII: F68VH75CJC)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74542-014-01	2 mL in 1 POUCH; Type 0: Not a Combination Product	06/19/2020
2	NDC: 74542-014-02	1 mL in 1 POUCH; Type 0: Not a Combination Product	06/19/2020
3	NDC: 74542-014-03	3 mL in 1 POUCH; Type 0: Not a Combination Product	06/19/2020
4	NDC: 74542-014-04	4 mL in 1 POUCH; Type 0: Not a Combination Product	06/19/2020
5	NDC: 74542-014-05	5 mL in 1 POUCH; Type 0: Not a Combination Product	06/19/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/19/2020

Labeler - Ningbo SKL International Co.,Ltd. (548277986)