Hand Sanitizer Gel by LS Promotions Inc. HAND SANITIZER GEL gel

Hand Sanitizer Gel by

Drug Labeling and Warnings

Hand Sanitizer Gel by is a Otc medication manufactured, distributed, or labeled by LS Promotions Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Drug Facts

Active Ingredients

Ethyl Alcohol 62%

Purpose

Antiseptic

Uses

• To help decrease bacteria on hands.

Warnings

• For external use only
• Flammable, keep away from fire or flame

When using this product

• Keep out of eyes
• In case of contact with eyes, flush thoroughly with water and then seek medical advise

Stop use and ask a doctor

• If irritation or redness develops

Keep out of reach of children

• If swallowed, get medical help or contact a poison control center immediately

Directions

• Place enough product in your palm to thoroughly cover hand.
• Rub hands together briskly until dry.
• For children under 6 years old, use adult supervision.

Other information

• Do not store above 100°F

Inactive Ingredients

Inactive ingredients: water, triethanolamine, carbomer, propylene glycol, fragrance, tocopherol acetate, aloe vera oil.

Questions or Comments?

Call weekdays from 9 AM to 5 PM EST at 631-231-2300

Principal display panel

ABL1211 Hand Sanitizer Gel 16 NDC: 72449-103-02

INGREDIENTS AND APPEARANCE

HAND SANITIZER GEL 
hand sanitizer gel gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72449-103
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.62 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
TRIETHANOLAMINE (UNII: 9O3K93S3TK)
FRAGRANCE GREEN APPLE ORC1902709 (UNII: X2H4PXN0HA)
ALOE VERA WHOLE (UNII: KIZ4X2EHYX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER 1342 (UNII: 809Y72KV36)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72449-103-06	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/04/2025
2	NDC: 72449-103-04	118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/04/2025
3	NDC: 72449-103-02	473 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	04/04/2025
4	NDC: 72449-103-05	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/04/2025
5	NDC: 72449-103-01	2.9 mL in 1 PACKET; Type 0: Not a Combination Product	04/04/2025
6	NDC: 72449-103-10	29 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/04/2025
7	NDC: 72449-103-11	295 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/04/2025
8	NDC: 72449-103-09	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/04/2025
9	NDC: 72449-103-08	236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	04/04/2025
10	NDC: 72449-103-07	295 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	04/04/2025
11	NDC: 72449-103-03	50 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/04/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	03/23/2020

Labeler - LS Promotions Inc. (024818391)

Registrant - LS Promotions Inc. (024818391)

Establishment
Name	Address	ID/FEI	Business Operations
LS Promotions Inc.		024818391	manufacture(72449-103)