HAND SANITIZER- ethyl alcohol gel

hand sanitizer by

Drug Labeling and Warnings

hand sanitizer by is a Otc medication manufactured, distributed, or labeled by Zhejiang Hongshiliang Health Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 65%

Purpose

Antiseptic

Use

Use To decrease bacteria on the skin

WARNINGS

Flammable. Keep away from fire or flame.
For external use only
When using this product do not use in or near the
eyes. In case of contact, rinse eyes thoroughly with
water. Stop use and ask a doctor if irritation or
rash appears and lasts.

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

Directions●wet hands thoroughly with product
and allow to dry without wiping●for children under 6,
use only under adult supervision●not recommended
for infants
Other information
●do not store above 110°F(43°C)
●may discolor some fabrics
●harmful to wood finishes and plastics

Inactive ingredients

Water, Carbomer,Triethanolamine, Aloe vera, Tocopheryl acetate,Glycerin, Fragrance

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75230-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	65 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
TOCOPHERYL RETINOATE (UNII: 0WN694NBMM)
CARBOMER 934 (UNII: Z135WT9208)
TRIETHANOLAMINE BENZOATE (UNII: M3EN4GC19W)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75230-001-01	60 in 1 CARTON	03/21/2020
1		1 in 1 BOX
1		37 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 75230-001-02	120 in 1 CARTON	03/21/2020
2		1 in 1 BOX
2		37 mL in 1 BOTTLE; Type 0: Not a Combination Product
3	NDC: 75230-001-03	3 in 1 CARTON	03/21/2020
3		60 in 1 CARTON
3		1 in 1 BOX
3		37 mL in 1 BOTTLE; Type 0: Not a Combination Product
4	NDC: 75230-001-04	18 in 1 CARTON	03/21/2020
4		153 mL in 1 BOTTLE; Type 0: Not a Combination Product
5	NDC: 75230-001-05	24 in 1 CARTON	03/21/2020
5		153 mL in 1 BOTTLE; Type 0: Not a Combination Product
6	NDC: 75230-001-06	30 in 1 CARTON	03/21/2020
6		153 mL in 1 BOTTLE; Type 0: Not a Combination Product
7	NDC: 75230-001-07	48 in 1 CARTON	03/21/2020
7		153 mL in 1 BOTTLE; Type 0: Not a Combination Product
8	NDC: 75230-001-08	18 in 1 CARTON	03/21/2020
8		307 mL in 1 BOTTLE; Type 0: Not a Combination Product
9	NDC: 75230-001-09	24 in 1 CARTON	03/21/2020
9		307 mL in 1 BOTTLE; Type 0: Not a Combination Product
10	NDC: 75230-001-10	54 in 1 CARTON	03/21/2020
10		153 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/21/2020

Labeler - Zhejiang Hongshiliang Health Technology Co., Ltd. (546641397)

Establishment
Name	Address	ID/FEI	Business Operations
Zhejiang Hongshiliang Health Technology Co., Ltd.		546641397	manufacture(75230-001)