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ADVANCE HAND SANITIZER MOISTURIZING FORMULA WITH ALOE AND VITAMIN E

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ADVANCE HAND SANITIZER MOISTURIZING FORMULA WITH ALOE AND VITAMIN E

Medically reviewed by . Last updated on Jan 1, 2020.

Dosage form: gel
Ingredients: ALCOHOL 70mL in 100mL
Labeler: All Pharma LLC
NDC Code: 53149-1120

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Active ingredient

Ethyl Alcohol 70.0%

Purpose

Antimicrobial

Uses

To help decrease bacteria on the skin. Recommended for repeat use.

Warnings

For external use only.

Flammable. Keep away from heat and flame.

When using this product

• Keep out of eyes. In case of contact, rinse eyes thoroughly with water

• Avoid contact with broken skin

• Do not inhale or ingest

Stop use and ask a doctor if

If irritation or redness develops.

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

Inactive ingredients

water, glycerin, propylene glycol,carbomer, fragrance, triethanolamine, isopropyl myristate, aloe barbadensis powder, tocopheryl acetate, FD&C Blue 1

ADVANCE HAND SANITIZER MOISTURIZING FORMULA WITH ALOE AND VITAMIN E 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53149-1120
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
CARBOMER 980 
GLYCERIN 
PROPYLENE GLYCOL 
ISOPROPYL MYRISTATE 
ALOE VERA LEAF 
TROLAMINE 
FD&C BLUE NO. 1 
ALPHA-TOCOPHEROL ACETATE 
Packaging
#Item CodePackage Description
1NDC:53149-1120-3946 mL in 1 BOTTLE
2NDC:53149-1120-1473 mL in 1 BOTTLE
3NDC:53149-1120-2354 mL in 1 BOTTLE
4NDC:53149-1120-4118 mL in 1 BOTTLE
5NDC:53149-1120-8236 mL in 1 BOTTLE
6NDC:53149-1120-53790 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E01/01/2020
Labeler - All Pharma LLC (078572520)
Registrant - All Pharma LLC (078572520)
Establishment
NameAddressID/FEIOperations
All Pharma LLC078572520manufacture(53149-1120)

Document Id: c824a473-9068-4339-ab02-2343aeb0840a Set id: 56860e2f-d49c-4b11-94bb-160bbc083c81 Version: 1 Effective Time: 20200101  All Pharma LLC

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