OTC Medication Information: U INSTANT HAND SANITIZER CLASSIC 2OZ

U INSTANT HAND SANITIZER CLASSIC 2OZ- alcohol gel
Universal Distribution Center LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Ethyl Alcohol 62.0 percent

Purpose

Antimicrobial

Uses

Hand Sanitizer to help reduce bacteria on skin.

WARNINGS

Flammable. Keep away from fire or flame.

For external use only.

When using this product,

do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water. Stop use and ask doctor if irritation or rash appears and lasts.

Keep out of reach for children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Place enough Product in your palm to thoroughly spread on both hands and rub into the skin until dry.
  • Children under 6 years of age should be supervised when using this product.

Other Information:

  • Store below 106 Fahrenheit (41 Degree Celsius)
  • May discolor certain fabrics or surfaces.

INACTIVE INGREDIENTS:

Water (Aqua), Aloe Barbadensis Leaf Juice, Carbomer, Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate (Vitamin E), triethanolamine.

label
(click image for full-size original)

U INSTANT HAND SANITIZER CLASSIC 2OZ
ethyl alcohol gel
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:52000-201
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALCOHOL (ALCOHOL) ALCOHOL 62 mL in 100 mL
Inactive Ingredients
Ingredient Name Strength
PROPYLENE GLYCOL
.ALPHA.-TOCOPHEROL ACETATE
ALOE VERA LEAF
CARBOMER 934
TRIETHANOLAMINE BENZOATE
GLYCERIN
WATER
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:52000-201-01 60 mL in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333A 05/01/2020
Labeler — Universal Distribution Center LLC (019180459)
Registrant — Universal Distribution Center LLC (019180459)

Revised: 05/2020 Universal Distribution Center 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.

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