BELUX LONDON HAND SANITIZER WITH ALOE VERA- alcohol gel

Belux London Hand Sanitizer with Aloe Vera by

Drug Labeling and Warnings

Belux London Hand Sanitizer with Aloe Vera by is a Otc medication manufactured, distributed, or labeled by Belux UK Medical Technology Ltd, Guangzhou Junchen Cosmetics Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Alcohol 75% (v/v)

Purpose

Antiseptic

Uses

To help decrease germs on the skin that could cause disease.

Recommended for repeated use.

Warnings

For external use only: hands

Flammable, keep away from fire or flame.

When using this product:

Avoid contact with broken skin.
Do not inhale or ingest.
Use with Caution if allergic.

When using this product:

Keep out of eyes. In case of contact with eyes, flush thoroughly with water.
Avoid contact with broken skin.
Do not inhale or ingest.
Use with Caution if allergic.

Stop use and ask a doctor if:

Irritation or redness develops.
Condition persists for more than 72 hours.

Keep out of reach by children:

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

Directions

Wet hands thoroughly without wiping until they dry.
For children under 6, use only under adult supervision.

Not recommended for infants.

Other information

After use, seal and tighten the cap and use product within the validity period.
After use, seal and keep away from light and moisture.

Store in a cool and dry place. Do not store above 37℃ (98.6℉)

Inactive ingredients

Aloe, Carbomer 940, Glycerin, Trolamine, Water.

Package Label - Principal Display Panel

100 mL NDC: 77084-001-01

300 mL NDC: 77084-001-02

500 mL NDC: 77084-001-03

INGREDIENTS AND APPEARANCE

BELUX LONDON HAND SANITIZER WITH ALOE VERA 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77084-001
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
GLYCERIN (UNII: PDC6A3C0OX)	1.55 mL  in 100 mL
ALOE (UNII: V5VD430YW9)	0.05 mL  in 100 mL
WATER (UNII: 059QF0KO0R)	19 mL  in 100 mL
CARBOMER 940 (UNII: 4Q93RCW27E)	0.4 mL  in 100 mL
TROLAMINE (UNII: 9O3K93S3TK)	4 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77084-001-01	100 mL in 1 BOTTLE, PLASTIC; Type 1: Convenience Kit of Co-Package	06/15/2020
2	NDC: 77084-001-02	300 mL in 1 BOTTLE, DISPENSING; Type 1: Convenience Kit of Co-Package	06/15/2020
3	NDC: 77084-001-03	500 mL in 1 BOTTLE, DISPENSING; Type 1: Convenience Kit of Co-Package	06/15/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/15/2020

Labeler - Belux UK Medical Technology Ltd (225838376)

Registrant - Belux UK Medical Technology Ltd (225838376)

Establishment
Name	Address	ID/FEI	Business Operations
Belux UK Medical Technology Ltd		225838376	repack(77084-001) , relabel(77084-001)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Junchen Cosmetics Co., Ltd.		402958582	manufacture(77084-001) , pack(77084-001) , label(77084-001)