62% V/V UNSCENTED- hand sanitizer gel

62% v/v Unscented by

Drug Labeling and Warnings

62% v/v Unscented by is a Otc medication manufactured, distributed, or labeled by Bell International Laboratories, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Alcohol 62% v/v

Purpose

Antiseptic

Uses

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

For external use only. Keep away from heat or flame.

Do not use: in children less than 2 months of age or in open skin wounds

When using this product keep out of eyes, ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Place enough product on hand to cover all surfaces. Rub hands together until dry.

Supervise children under 6 years of age when using this product and avoid swallowing.

Other Information

Store between 15-30 C (59-86 F).

Avoid freezing and excessive heat above 40 C (104 F)

Inactive Ingredients

Water, Glycerin, Hydroxypropyl Guar, Citric Acid, Calendula Officinalis Flower Extract, Chamomilla Recutita Flower Extract, Aloe Barbadensis Leaf Juice

principal display panel

INGREDIENTS AND APPEARANCE

62% V/V UNSCENTED 
hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76150-245
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
GUARAPROLOSE (1300 MPA.S AT 1%) (UNII: 1530WMS90S)
CHAMOMILE (UNII: FGL3685T2X)
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76150-245-50	3 mL in 1 PACKET; Type 0: Not a Combination Product	05/08/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/08/2020

Labeler - Bell International Laboratories, Inc. (967781555)