Hand Sanitizer PL0591 PL1808

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Broder Bros Co.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

HAND SANITIZER- alcohol gel 
Broder Bros Co.

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Hand Sanitizer PL0591 PL1808

Drug Facts

Active ingredient

Alcohol 62%

Purpose

Antiseptic

Use

For handwashing to decrease bacteria on skin

Warnings

Flammable. Keep away from fire and flame.

For external use only

When using this product

• Keep out of eyes.
• In the case of contact with eyes flush thoroughly with water.
• Avoid contact with broken skin.
• Do not inhale or ingest.

Stop use & ask doctor if

irritation and redness develops and persists for more than 72 hours.

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center immediately

Directions

• Wet hands thoroughly with product, briskly rub together until dry.
• Always supervise children in use of this product.
• Children under 6 months of age: Ask a doctor.

Other information

• Store at 68°F to 77°F (20°C to 25°C).

Inactive Ingredients

Carbopol 940, Fragrance, Triethanolamine, Water.

Questions?

1-800-873-7746 M-F 8am-5pm EST

Hand Sanitizer

Net. wt. 2.19 Fl. oz. (65mL)

Lot no: Use by:

Made in China

Dist. by: Broder Bros. Co., dba Prime Line

Bridgeport, CT 06610/Gaffney, SC 29341

HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71513-102
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
TROLAMINE (UNII: 9O3K93S3TK)
CARBOMER 940 (UNII: 4Q93RCW27E)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71513-102-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2020	07/31/2023
2	NDC: 71513-102-08	65 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2020	10/15/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	01/01/2020	10/15/2023

Labeler - Broder Bros Co. (107044246)

Revised: 1/2024

Document Id: 09aba42f-d98f-32f8-e063-6294a90aead4

34390-5

Set id: d4b45a38-4e81-9dcb-e053-2a95a90aa576

Version: 3

Effective Time: 20240101