JNK YRD ADVANCED HAND SANITIZER LAVENDER SCENT- alcohol liquid

JNK YRD Advanced Hand Sanitizer LAVENDER SCENT by

Drug Labeling and Warnings

JNK YRD Advanced Hand Sanitizer LAVENDER SCENT by is a Otc medication manufactured, distributed, or labeled by Zhejiang iColor Biotech Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Ethyl Alcohol 75% v/v

Purpose

Antiseptic

Uses[s]

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

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

Do not use

• in children less than 2 months of age
• 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 conditions.

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

• Store between 15-30°C (59-86°F)
• Avoid freezing and excessive heat above 40°C (104°F)

Inactive ingredients

Purified Water USP, Glycerin, Panthenol, Tocopheryl Acetate

Package Labeling: 60ml

Package Labeling: 500ml

INGREDIENTS AND APPEARANCE

JNK YRD ADVANCED HAND SANITIZER LAVENDER SCENT 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74934-088
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PANTHENOL (UNII: WV9CM0O67Z)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74934-088-01	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/10/2021	01/31/2026
2	NDC: 74934-088-02	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/10/2021	01/31/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	08/10/2021	01/31/2026

Labeler - Zhejiang iColor Biotech Co., Ltd (554528308)