Dermasil Hand Sanitizer Unscented

Dosage form: liquid
Ingredients: alcohol 70mL in 100mL
Labeler: Fantasia Beauty LLC
NDC code: 76184-0701

Medically reviewed by Drugs.com. Last updated on Jun 16, 2023.

Drug Facts

Active ingredient

Alcohol 70%

Purpose

Antiseptic

Uses

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

For external use only.

Flammable, keep away from fire and flame.

Do not use

on children less than 2 months of age
on open skin wounds

When using this product

keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water

Stop use and ask a doctor if irritation and redness develops and persists.

Keep out of reach of children.

If swallowed, contact a doctor or Poison Control Center right away.

Directions

Apply a dime sized amount to hands. Rub hands together until dry.
Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

Store between 59-86°F.

Avoid freezing and excessive heat above 104°F.

Inactive ingredients

Water/Aqua/Eau, Glycerin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Fragrance/Parfum, Triethanolamine, Aloe Barbadensis Extract, Tocopheryl Acetate.

Principal Display Panel – 100 mL Bottle

Dermasil®
LABS

Pharmaceutical Research

Kills 99.99% of Most Germs

Effective in Just 30 Seconds

Includes Skin Conditioners

Dermasil®
Hand Sanitizer
UNSCENTED

3.4 FL.OZ. (100 mL)

DERMASIL HAND SANITIZER UNSCENTED
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:76184-0701
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
aloe vera leaf
glycerin
water
carbomer interpolymer type a (55000 cps)
trolamine
.alpha.-tocopherol acetate

Packaging
#	Item Code	Package Description
1	NDC:76184-0701-2	100 mL in 1 BOTTLE, PLASTIC
2	NDC:76184-0701-1	30 mL in 1 BOTTLE, PLASTIC
3	NDC:76184-0701-3	220 mL in 1 BOTTLE, PLASTIC
4	NDC:76184-0701-5	500 mL in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/22/2020

Labeler - Fantasia Beauty LLC (037273190)

Document Id: d18373f3-71e8-4f0d-a638-27a2a9abff15

Set id: 1987cecd-95c2-45eb-be14-a8c99ee067e3

Version: 3

Effective Time: 20200626

Fantasia Beauty LLC

Further information

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

Medical Disclaimer