MU Instant Hand Sanitizer: Package Insert and Label Information

MU INSTANT HAND SANITIZER- alcohol gel
Ningbo Royal Union 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.

Active Ingredient

Alcohol Denat. 75% v/v.

Purpose

Antiseptic

Uses

  • to decrease bacteria on the skin that could cause disease.
  • recommended for repeated use.

Warnings

For external use only. Flammable. Keep away from fire or flame.
When using this product, avoid contact with broken skin, do not inhale or ingest.
Do not use in the eyes. In case of contact, rinse eyes thoroughly with water.
Stop use and ask a doctor if

  • irritation or redness develops
  • condition persists for more than 72 hours.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

•Place enough product on hands to cover all surfaces. Rub hands together until dry.
•Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

Other information

  • Do not store above 105°F.
  • May discolor some fabrics.
  • Harmful to wood finishes and plastics.

Inactive ingredients

Water, acrylic acid homopolymer, Butane-1,3-diol, 1,1-propanediol, monoisobutanolamine, Fragrance

Package Label — Principal Display Panel

Product label
(click image for full-size original)

MU INSTANT HAND SANITIZER
alcohol gel
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:78422-001
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALCOHOL (ALCOHOL) ALCOHOL 75 mL in 100 mL
Inactive Ingredients
Ingredient Name Strength
WATER
POLYACRYLIC ACID (250000 MW)
BUTYLENE GLYCOL
PROPYLENE GLYCOL
AMINOMETHYLPROPANOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:78422-001-01 10 mL in 1 BOTTLE, PLASTIC None
2 NDC:78422-001-02 20 mL in 1 BOTTLE, PLASTIC None
3 NDC:78422-001-03 30 mL in 1 BOTTLE, PLASTIC None
4 NDC:78422-001-04 45 mL in 1 BOTTLE, PLASTIC None
5 NDC:78422-001-05 50 mL in 1 BOTTLE, PLASTIC None
6 NDC:78422-001-06 55 mL in 1 BOTTLE, PLASTIC None
7 NDC:78422-001-07 60 mL in 1 BOTTLE, PLASTIC None
8 NDC:78422-001-08 80 mL in 1 BOTTLE, PLASTIC None
9 NDC:78422-001-09 100 mL in 1 BOTTLE, PLASTIC None
10 NDC:78422-001-10 120 mL in 1 BOTTLE, PLASTIC None
11 NDC:78422-001-11 180 mL in 1 BOTTLE, PLASTIC None
12 NDC:78422-001-12 200 mL in 1 BOTTLE, PLASTIC None
13 NDC:78422-001-13 237 mL in 1 BOTTLE, PLASTIC None
14 NDC:78422-001-14 250 mL in 1 BOTTLE, PLASTIC None
15 NDC:78422-001-15 300 mL in 1 BOTTLE, PLASTIC None
16 NDC:78422-001-16 474 mL in 1 BOTTLE, PLASTIC None
17 NDC:78422-001-17 500 mL in 1 BOTTLE, PLASTIC None
18 NDC:78422-001-18 946 mL in 1 BOTTLE, PLASTIC None
19 NDC:78422-001-19 1000 mL in 1 BOTTLE, PLASTIC None
20 NDC:78422-001-20 2000 mL in 1 BOTTLE, PLASTIC None
21 NDC:78422-001-21 3000 mL in 1 BOTTLE, PLASTIC None
22 NDC:78422-001-22 4000 mL in 1 BOTTLE, PLASTIC None
23 NDC:78422-001-23 5000 mL in 1 BOTTLE, PLASTIC None
24 NDC:78422-001-24 10000 mL in 1 BOTTLE, PLASTIC None
25 NDC:78422-001-25 20000 mL in 1 BOTTLE, PLASTIC None
26 NDC:78422-001-26 50000 mL in 1 BOTTLE, PLASTIC None
27 NDC:78422-001-27 100000 mL in 1 BOTTLE, PLASTIC None
28 NDC:78422-001-28 980 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 05/20/2020
Labeler — Ningbo Royal Union Co., Ltd. (529255035)

Revised: 05/2020 Ningbo Royal Union Co., Ltd.

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