INSTANT HAND SANITIZER gel

Instant Hand Sanitizer by

Drug Labeling and Warnings

Instant Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by SINGWONG ASIA PACIFIC (BOLUO) CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Alcohol 76% v/v. Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer

Use

Hand Sanitizer to help reduce bacteria on skin.

Warnings

Flammable. Keep away from heat or flame

For external use only

For external use only

stop use and ask a doctor if

irritation or rash appears and lasts

when using this product

When using this product do not use in or near the eyes,in case of contact, rinse eyes thoroughly with water.

STOP USE

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

put enough product in your palm to cover hands and rub hands together briskly until dry.

children under 6 years of age should be supervised.

Other information

• Store below 86F/30C
• May discolor certain fabrics or surfaces

Inactive ingredients

water,glycerin,sodium polyacylate(2500000MW),aloe

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

INSTANT HAND SANITIZER 
instant hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75283-006
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
SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE (UNII: V5VD430YW9)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75283-006-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/17/2020
2	NDC: 75283-006-02	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/17/2020
3	NDC: 75283-006-03	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/17/2020
4	NDC: 75283-006-04	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/17/2020
5	NDC: 75283-006-05	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/17/2020
6	NDC: 75283-006-06	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/17/2020
7	NDC: 75283-006-07	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/17/2020
8	NDC: 75283-006-08	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/17/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/17/2020

Labeler - SINGWONG ASIA PACIFIC (BOLUO) CO., LTD. (546342424)

Establishment
Name	Address	ID/FEI	Business Operations
SINGWONG ASIA PACIFIC (BOLUO) CO., LTD.		546342424	manufacture(75283-006)