ADVANCED HAND SANITIZER- ethyl alcohol gel

Advanced Hand Sanitizer by

Drug Labeling and Warnings

Advanced 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 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 105⁰F
• 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 or acrylates/C10-30 alkyl acrylate crosspolymer, fragrance, benzophenone-4, blue 1, yellow 5

Disclaimer

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

EMPLOYY-OWNED

Advrse 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 WITH ALOE

Kills more than 99.99% of Germs*

with added moisturizers

33.8 FL OZ (1L) 1.05 QT

INGREDIENTS AND APPEARANCE

ADVANCED HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83986-439
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 CAPRYLATE/CAPRATE (UNII: G7515SW10N)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)
SULISOBENZONE (UNII: 1W6L629B4K)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83986-439-16	59 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	02/23/2024
2	NDC: 83986-439-34	236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	02/23/2024
3	NDC: 83986-439-86	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/23/2024
4	NDC: 83986-439-32	355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/23/2024
5	NDC: 83986-439-50	709 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/23/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	02/23/2024

Labeler - UpLift Brands LLC (119091527)

Registrant - Consumer Product Partners, LLC (119091520)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091520	manufacture(83986-439)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091514	manufacture(83986-439)