HAND SANITIZER- alcohol gel

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by HAIAN KANGRUI TEXTILE CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 62%

Purpose

Antiseptic

Uses

For hand sanitizing to reduce bacteria on the skin.

Warnings

For external use only.

Flammable. Keep away from fire and flame.

When using this product，

do not use in or near the eyes.In case of contact，rinse eyes thoroughly with water.

Discontinue use

if irritation or redness develops.

Keep out of reach of children.

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

Directions

Squeeze small amount in your palm and briskly rub hands together until dry.

Inactive ingredients

Water, Glycerin, Carbomer, Fragrance, Triethanolamine, Aloe Barbadensis Leaf Juice, Vitamin E, Iron Oxide(CI 77499), Iron Oxide(CI 77492), D&C RED NO. 30

87001-002-01

87001-002-02

87001-002-03

87001-002-04

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87001-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 g  in 112 mL

Inactive Ingredients
Ingredient Name	Strength
CARBOMER INTERPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 132584PQMO)
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
FERROSOFERRIC OXIDE (UNII: XM0M87F357)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
TROLAMINE (UNII: 9O3K93S3TK)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
D&C RED NO. 30 (UNII: 2S42T2808B)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87001-002-01	15 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/12/2025
2	NDC: 87001-002-02	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/12/2025
3	NDC: 87001-002-03	54 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/12/2025
4	NDC: 87001-002-04	15 mL in 1 BOTTLE; Type 1: Convenience Kit of Co-Package	08/12/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	08/12/2025

Labeler - HAIAN KANGRUI TEXTILE CO., LTD. (560687104)

Establishment
Name	Address	ID/FEI	Business Operations
HAIAN KANGRUI TEXTILE CO., LTD.		560687104	manufacture(87001-002)