OTC Medication Information: M MARVEL SANI CARE Multi Function Disinfectant Liquid No Rinse

M MARVEL SANI CARE MULTI FUNCTION DISINFECTANT LIQUID NO RINSE- benzalkonium chloride spray
GUANGZHOU TECHIN DEVELOPMENT 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

Benzalkonium Chloride 0.02%

Purpose

Antiseptic

Use

For Daily and Surgical hand disinfection to reduce bacteria on hands

Warnings

For external use only.
Keep away from fires and high temperatures.

Do Not Use: On open skin wounds.

When using this product: Avoid eyes.
In case of contact with eyes, rinse eyes thoroughly with water.

Stop use If irritation or rash occurs. If condition persists, contact a health care practitioner.

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

Directions

  • Put proper amount (around 3ml) onto palm and rub hands briskly until dry.
  • No washing or rinsing required. Air dries quickly.

Other information

Keep in closed container in a cool dry place of ambient temperature.
Batch and MFG date printed on bottle.
Validity: 24 months from MFG date.
MADE IN CHINA

Inactive ingredients

Didecyl Dimethyl Ammonium Chloride, Ethyl Alcohol, Disodium EDTA, Water

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M MARVEL SANI CARE MULTI FUNCTION DISINFECTANT LIQUID NO RINSE
benzalkonium chloride spray
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:80107-003
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE 0.02 g in 100 mL
Inactive Ingredients
Ingredient Name Strength
WATER
ALCOHOL
DISODIUM HEDTA
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:80107-003-01 60 mL in 1 BOTTLE None
2 NDC:80107-003-02 250 mL in 1 BOTTLE None
3 NDC:80107-003-03 500 mL in 1 BOTTLE None
4 NDC:80107-003-04 750 mL in 1 BOTTLE None
5 NDC:80107-003-05 1000 mL in 1 BOTTLE None
6 NDC:80107-003-06 3785 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 12/21/2020
Labeler — GUANGZHOU TECHIN DEVELOPMENT CO., LTD (527219392)
Establishment
Name Address ID/FEI Operations
GUANGZHOU TECHIN DEVELOPMENT CO., LTD 527219392 manufacture (80107-003)

Revised: 01/2021 GUANGZHOU TECHIN DEVELOPMENT 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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