MOISTURIZING HAND SANITIZER- ethyl alcohol gel

Moisturizing Hand Sanitizer by

Drug Labeling and Warnings

Moisturizing 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]

Claims

germ-x

PRO

MOISTURIZING

FOAMING HAND SANITIZER

Active ingredient

Ethyl alcohol 62%

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
• 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 105°F 
• may discolor some fabrics
• harmful to wood finishes and plastics

Inactive ingredients

water, PEG-8 dimethicone, meadowfoamamidopropyl betaine, glycerin, tocopheryl acetate, isopropyl myristate

Adverse Reactions

DISTRIBUTED BY: UPLIFT BRANDS, LLC

ST. LOUIS, MO 63114

1-866 MY GERMX

DSP-TN-21091 DSP-MO-20087

Principal display panel

germ-X ®

PRO

MOISTURIZING

FOAMING

HAND SANITIZER

1150 mL (1.21 QT) 39 FL OZ

INGREDIENTS AND APPEARANCE

MOISTURIZING HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83986-447
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PEG-8 DIMETHICONE (UNII: GIA7T764OD)
MEADOWFOAMAMIDOPROPYL BETAINE (UNII: HNV0L650LG)
GLYCERIN (UNII: PDC6A3C0OX)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83986-447-45	1150 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/12/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505(a)(3)	04/12/2024

Labeler - UpLift Brands, LLC (119091527)

Registrant - Consumer Product Partners, LLC (119091520)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091520	manufacture(83986-447)