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 Type HUMAN OTC DRUG Item Code (Source) NDC:53149-1120 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   CARBOMER 980   GLYCERIN   PROPYLENE GLYCOL   ISOPROPYL MYRISTATE   ALOE VERA LEAF   TROLAMINE   FD&C BLUE NO. 1   ALPHA-TOCOPHEROL ACETATE

Packaging # Item Code Package Description 1 NDC:53149-1120-3 946 mL in 1 BOTTLE 2 NDC:53149-1120-1 473 mL in 1 BOTTLE 3 NDC:53149-1120-2 354 mL in 1 BOTTLE 4 NDC:53149-1120-4 118 mL in 1 BOTTLE 5 NDC:53149-1120-8 236 mL in 1 BOTTLE 6 NDC:53149-1120-5 3790 mL in 1 BOTTLE

Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 01/01/2020

Labeler - All Pharma LLC (078572520)

Registrant - All Pharma LLC (078572520)

Establishment
Name	Address	ID/FEI	Operations
All Pharma LLC		078572520	manufacture(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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Medical Disclaimer