OTC Medication Information: Advanced Hand Sanitizer

ADVANCED HAND SANITIZER- alcohol gel
UpLift Brands LLC

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

image description
(click image for full-size original)
ADVANCED HAND SANITIZER
ethyl alcohol gel
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:83986-439
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALCOHOL (ALCOHOL) ALCOHOL 70 mL in 100 mL
Inactive Ingredients
Ingredient Name Strength
WATER
ALOE VERA LEAF
GLYCERYL CAPRYLATE/CAPRATE
GLYCERIN
ISOPROPYL MYRISTATE
.ALPHA.-TOCOPHEROL ACETATE
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S)
SULISOBENZONE
FD&C BLUE NO. 1
FD&C YELLOW NO. 5
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:83986-439-16 59 mL in 1 BOTTLE, DISPENSING None
2 NDC:83986-439-34 236 mL in 1 BOTTLE, PUMP None
3 NDC:83986-439-86 1000 mL in 1 BOTTLE, PLASTIC None
4 NDC:83986-439-32 355 mL in 1 BOTTLE, PLASTIC None
5 NDC:83986-439-50 709 mL in 1 BOTTLE, PLASTIC None
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 Operations
Consumer Product Partners, LLC 119091520 manufacture (83986-439)
Establishment
Name Address ID/FEI Operations
Consumer Product Partners, LLC 119091514 manufacture (83986-439)

Revised: 02/2024 UpLift Brands LLC

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Terms of Use | Copyright © 2024. All Rights Reserved.