HAND SANITIZER- hand sanitizer gel
LS Promotions Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Hand Sanitizer Gel

Drug Facts

Active Ingredients

Ethyl Alcohol

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, glycerin, propylene glycol, carbomer, triethanolamine, isopropyl myristate, aloe vera oil, fragrance

Questions or Comments?

Call weekdays from 9 AM to 5 PM EST at 631-231-2300 - www.lancopromo.com

Principal display panel

ABL1900 Hand Sanitizer Gel NDC # 72449-100-03

HAND SANITIZER
hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:72449-100
Route of Administration	TOPICAL

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

Ingredient Name	Strength
Inactive Ingredients
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER 1342 (UNII: 809Y72KV36)
TROLAMINE (UNII: 9O3K93S3TK)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
WATER (UNII: 059QF0KO0R)
ALOE VERA WHOLE (UNII: KIZ4X2EHYX)
GLYCERIN (UNII: PDC6A3C0OX)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:72449-100-03	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/23/2020
2	NDC:72449-100-04	118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/23/2020
3	NDC:72449-100-05	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/23/2020
4	NDC:72449-100-06	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/23/2020
5	NDC:72449-100-01	2.9 mL in 1 PACKET; Type 0: Not a Combination Product	03/23/2020
6	NDC:72449-100-02	5.9 mL in 1 PACKET; Type 0: Not a Combination Product	03/23/2020
7	NDC:72449-100-07	29 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/23/2020
8	NDC:72449-100-08	295 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/23/2020
9	NDC:72449-100-09	354 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	03/23/2020
10	NDC:72449-100-10	3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/23/2020
11	NDC:72449-100-11	946 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	12/01/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	03/23/2020

Labeler - LS Promotions Inc. (024818391)

Registrant - LS Promotions Inc. (024818391)

Name	Address	ID/FEI	Business Operations
Establishment
LS Promotions Inc.		024818391	manufacture(72449-100)