ADVANCED HAND SANITIZER WITH ALOE- ethyl alcohol gel

Advanced Hand Sanitizer with Aloe by

Drug Labeling and Warnings

Advanced Hand Sanitizer with Aloe 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 fire or 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 develop
• conditon 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 105⁰ F
• may discolor some fabrics
• harmful to wood finishes and plastics

Inactive ingredients

water, Aloe barbadensis leaf juice, glyceryl caprylate/caprate, glycerin, isopropyl myristate, tocopheryl acetate, carbomer, fragrance

Disclaimer

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

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

FORMULA MADE INUSA

EMPLOYEE OWNED

Adverse reaction

Dist. By Vi-Jon, LLC.

8515 Page Ave., St. Louis, MO 63114

Principal display panel

germ-x ®

SINCE 1997

ADVANCED

moisturizing hand sanitizer

with Aloe & Vitamin E

Kills more than 99.99% of germs in 15 seconds*

70% ETHYL ALCOHOL

FORMULA MADE IN USA

EMPLOYEE OWNED

12 FL OZ (354 ML)

INGREDIENTS AND APPEARANCE

ADVANCED HAND SANITIZER WITH ALOE 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83986-996
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)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERYL MONOCAPRYLOCAPRATE (UNII: G7515SW10N)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83986-996-32	355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/02/2020
2	NDC: 83986-996-48	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/02/2020
3	NDC: 83986-996-08	3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/02/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	12/02/2020

Labeler - UpLift Brands, LLC (119091527)

Registrant - Consumer Product Partners, LLC (119091520)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091520	manufacture(83986-996)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091514	manufacture(83986-996)