HAND SANITIZER- ethyl alcohol gel

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by UpLift Brands LLC, Consumer Product Partners, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl alcohol 70%

Purpose

Antiseptic

Uses

• to decrease bacteria on the skin that could cause disease
• recommended for repeated use

Warnings

For external use only: hands

Flammable.  Keep away from heat and flame.

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

Stop use and ask a doctor if

• irritation and redness develops
• condition persists for more than 72 hours

Keep out of reach of children.

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

Directions

• wet hands thoroughly with product and allow to dry without wiping
• for children under 6, use only under adult supervision
• not recommended for infants

Other information

• do not store above 105⁰F
• may discolor some fabrics
• harmful to wood finishes and plastics

Inactive ingredients

water, glyceryl caprylate/caprate, glycerin, isopropyl myristate, tocopheryl acetate, carbomer or acrylates/C10-30 alkyl acrylate crosspolymer, fragrance, benzophenone-4

Disclaimer

DSP-TN-21091 DSP-MO-20087 DSP-MO-28 DSD-MO-20068

*Effective at eliminating more than 99.99% of many common harmful germs and bacteria in as little as 15 seconds.

FORMULA MADE IN USA

EMPLOYEE OWNED

Adverse reaction

Dist. by: Vi-Jon, LLC 8515 Page Ave

St. Louis, MO 63114

Principal display panel

germ-x®

since 1997

ADVANCED

70% alcohol hand sanitizer

Kills more than 99.99% of Germs*

with added moisturizers

33.8 FL OZ (1L) 1.05QT

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83986-529
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERYL CAPRYLATE/CAPRATE (UNII: G7515SW10N)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36)
SULISOBENZONE (UNII: 1W6L629B4K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83986-529-16	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/22/2022
2	NDC: 83986-529-34	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/22/2022
3	NDC: 83986-529-32	355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/22/2022
4	NDC: 83986-529-50	710 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/22/2022
5	NDC: 83986-529-86	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/22/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M505G(a)(3)	12/22/2022

Labeler - UpLift Brands LLC (119091527)

Registrant - Consumer Product Partners, LLC (119091520)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091520	manufacture(83986-529)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091514	manufacture(83986-529)