OTC Medication Information: M and U Make You Up Hand Sanitizer

M AND U MAKE YOU UP HAND SANITIZER- alcohol gel
Idea Beautify Industry Co., Ltd.

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.

Drug Facts

Active ingredient

Alcohol 75% v/v

Purpose

Antiseptic

Use

for hand-washing to decrease bacteria on the skin, only when water is not available

Warnings

  • Flammable, keep away from fire and flame
  • For external use only

When using this product

  • Do not get into eyes. If contact occurs, rinse eyes thoroughly with water.
  • May discolor some fabrics.

Stop use and ask a doctor if

  • Irritation and redness develop.

Keep out of reach of children.

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

Directions

wet hands thoroughly with productand allow to dry without wiping

Other information

store below 105° F

Inactive ingredients

Water (Aqua), Glycerin, Aloe Barbadensis Leaf Juice, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Potassium Sorbate, Sodium Benzoate, Citric Acid, Fragrance (Parfum), Sodium Bicarbonate, Denatonium Benzoate.

Questions?

+1-800-424-9300

Package Labeling:

Label
(click image for full-size original)

M AND U MAKE YOU UP HAND SANITIZER
alcohol gel
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:79469-001
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALCOHOL (ALCOHOL) ALCOHOL 0.75 mL in 1 mL
Inactive Ingredients
Ingredient Name Strength
WATER
GLYCERIN
ALOE VERA LEAF
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)
POTASSIUM SORBATE
SODIUM BENZOATE
CITRIC ACID MONOHYDRATE
SODIUM BICARBONATE
DENATONIUM BENZOATE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:79469-001-01 500 mL in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333E 07/10/2020
Labeler — Idea Beautify Industry Co., Ltd. (553560617)

Revised: 10/2020 Idea Beautify Industry Co., Ltd.

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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