OTC Medication Information: M Skin Care Gel Hand Sanitizer 120

M SKIN CARE GEL HAND SANITIZER 120- alcohol gel
Mingshi Technology 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 70%

­­­­­­­­­­­­­­­­­­­­­ Purpose

Antiseptic

Uses

To help reduce bacteria on the skin.

Warnings

FLAMMABLE. Keep away from heat or flame

For External Use only. When using this product

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

Do not use with children less than 2 months of age- On open skin wounds -around eyes -in ears and mouth.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center immediately

Directions

Apply enough product on hands to cover all surfaces. Rub hands together until dry.

Inactive Ingredients

Water, Aloe Barbadensis, Acrylates/C10-30 Alkylacrylate crosspolymer, Triethanolamine, Tocopheryl acetate, Glycerin, Fragrance

Other Information

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

M Skin Care Gel Hand Sanitizer Anti-Bacterial 120ml

120

M SKIN CARE GEL HAND SANITIZER 120
alcohol 70% gel
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:73992-102
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALCOHOL (ALCOHOL) ALCOHOL 84 mL in 120 mL
Inactive Ingredients
Ingredient Name Strength
WATER
ALOE VERA LEAF
GLYCERIN
TROLAMINE
(C10-C30)ALKYL METHACRYLATE ESTER
ALPHA-TOCOPHEROL ACETATE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:73992-102-04 120 mL in 1 BOTTLE None
2 NDC:73992-102-02 60 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 03/02/2020
Labeler — Mingshi Technology Co., LTD (542992088)
Registrant — Mingshi Technology Co., LTD (542992088)

Revised: 03/2020 Mingshi Technology 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.

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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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