84641-002 (Hand Sanitizer )

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by NANTONG QINJI HEALTH TECHNOLOGY CO., LTD, NANTONG QINJI HEALTH TECHNOLOGY CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

HAND SANITIZER- alcohol gel 
NANTONG QINJI HEALTH TECHNOLOGY CO., LTD

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84641-002 (Hand Sanitizer)

Active ingredients

Ethyl Alcohol 62%

Purpose

Antiseptic

Uses

For hand sanitizing to reduce bacteria on the skin.

Warinings

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.

84641-002-01

84641-002-02

84641-002-03

HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84641-002
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
FERROSOFERRIC OXIDE (UNII: XM0M87F357)
D&C RED NO. 30 (UNII: 2S42T2808B)
TROLAMINE (UNII: 9O3K93S3TK)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
CARBOMER INTERPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 132584PQMO)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84641-002-01	15 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/12/2024
2	NDC: 84641-002-02	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/12/2024
3	NDC: 84641-002-03	54 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/12/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	08/12/2024	08/20/2024

Labeler - NANTONG QINJI HEALTH TECHNOLOGY CO., LTD (450420747)

Establishment
Name	Address	ID/FEI	Business Operations
NANTONG QINJI HEALTH TECHNOLOGY CO., LTD.		450420747	manufacture(84641-002)

Revised: 8/2024

Document Id: 2013f1e9-94f3-348f-e063-6394a90aa948

34390-5

Set id: 1f9ea65c-bd8e-e25b-e063-6294a90a0d20

Version: 3

Effective Time: 20240819