AMBER OUD WOOD HAND SANITIZER liquid

Amber Oud Wood Hand Sanitizer by

Drug Labeling and Warnings

Amber Oud Wood Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Zhejiang Meimi Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Ethyl Alcohol 70% v/v

Purpose

Antimicrobial

Use

Hand sanitizer to help reduce bacteria on the skin that may cause disease.

Warnings

• for external use only.
• Flammable.
• Keep away from heat and flame.

STOP USE

Stop use and ask a doctor if·irritation or redness develops.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children·
if swallowed, get medical help or contact a Poison Control Center.

Directions

Spray enough product in your palm to thoroughly cover your hands. Rub hands together briskly until dry. Recommended for repeated use. Children under 6 years of age should be supervised when using this product.

Inactive ingredients

Water(Aqua), Fragrance(Parfum), Glycerin, Hexyl Cinnamal, Limonene, Linalool, Yellow 6, Blue 1, Yellow 5.

WHEN USING

When using this product·
avoid contact with face, eyes, and broken skin. In case of eye contact, flush with plenty of water and seek medical advice.

Package Label - Principal Display Panel

45 mL in 1 BOTTLE

NDC: 41366-091-01

INGREDIENTS AND APPEARANCE

AMBER OUD WOOD HAND SANITIZER 
amber oud wood hand sanitizer liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 41366-091
Route of Administration	EXTRACORPOREAL

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
HEXYL CINNAMAL (UNII: 7X6O37OK2I)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
BLUE 1 (UNII: H3R47K3TBD)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
YELLOW 5 (UNII: I753WB2F1M)
LINALOOL (UNII: D81QY6I88E)
YELLOW 6 (UNII: H77VEI93A8)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 41366-091-01	45 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/10/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	06/10/2025

Labeler - Zhejiang Meimi Technology Co., Ltd. (413668440)

Establishment
Name	Address	ID/FEI	Business Operations
Zhejiang Meimi Technology Co., Ltd.		413668440	manufacture(41366-091)