OTC Medication Information: MA MAGIC ARMOUR Hand and Skin Sanitizer

MA MAGIC ARMOUR HAND AND SKIN SANITIZER- alcohol liquid
Ay-tu Plastik Ambalaj Sanayi Ve Ticaret Limited Sirketi

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[s]

Ethyl Alcohol 80% w/w

Purpose

Antiseptic

Use[s]

■ 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 heat or flame.

Do not use

■ In children less than 2 months of age

■ On open skin wounds

When using this productkeep 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 or rash occurs.

Keep out of reach of children If swallowed, get medical help or contact 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

Store between 15-30°C (59-86F) Avoid freezing and excessive heat above 40°C (104F)

Inactive Ingredients

Deionized water, glycerine, hydrogen peroxide

Kills 99,99% of germs!

Alcohol-Based

MANUFACTURED FOR

AYTU PLASTİK

Minareliçavuş Mah.

Etkin Sok. No. 12

Nilüfer Bursa / TURKEY

Packaging

untitled
(click image for full-size original)

MA MAGIC ARMOUR HAND AND SKIN SANITIZER
ethyl alcohol liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:78373-001
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALCOHOL (ALCOHOL) ALCOHOL 0.8 mL in 1 mL
Inactive Ingredients
Ingredient Name Strength
WATER
GLYCERIN
HYDROGEN PEROXIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:78373-001-01 100 mL in 1 BOTTLE None
2 NDC:78373-001-02 250 mL in 1 BOTTLE None
3 NDC:78373-001-05 500 mL in 1 BOTTLE None
4 NDC:78373-001-10 1000 mL in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333A 05/29/2020
Labeler — Ay-tu Plastik Ambalaj Sanayi Ve Ticaret Limited Sirketi (355625702)

Revised: 05/2020 Ay-tu Plastik Ambalaj Sanayi Ve Ticaret Limited Sirketi

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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