Morlii Antibacterial Hand Sanitizer by Sonchin Biomedical Cosmetics Corp. Sonchin 015-01

Morlii Antibacterial Hand Sanitizer by

Drug Labeling and Warnings

Morlii Antibacterial Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Sonchin Biomedical Cosmetics Corp.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

MORLII ANTIBACTERIAL HAND SANITIZER- alcohol spray 
Sonchin Biomedical Cosmetics Corp.

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.

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Sonchin 015-01

Active Ingredient(s)

Ethyl Alcohol 75% v/v

Purpose

Antibacterial

Use

  • Helps reduce bacteria on the skin
  • Recommended for repeated use

Warnings

For external use only.

Flammable. Keep away from fire or flame.

Do not use

  • on children less than 2 months of age
  • on open skin wounds
  • around eyes
  • in ears and mouth

When using this product

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

  • avoid contact with broken skin
  • do not inhale or ingest

Stop use and ask a doctor

if irritation or rash occurs.

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

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

Inactive ingredients

PURIFIED WATER ,GLYCERINE, PROPYLENE, GLYCOL, ALOE BARBADENSIS LEAF JUICE, SUCROSE OCTAACETATE, TERT-BUTYL ALCOHOL

Package Label - Principal Display Panel

100 ml NDC: 73662-015-01 100ml_label

MORLII ANTIBACTERIAL HAND SANITIZER 
alcohol spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 73662-015
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL75 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
2-PHENYLPROPANAL PROPYLENE GLYCOL ACETAL (UNII: 1ZRR9A405A)  
WATER (UNII: 059QF0KO0R)  
SUCROSE OCTAACETATE (UNII: 07V591057T)  
TERT-BUTYL ALCOHOL (UNII: MD83SFE959)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 73662-015-01100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product11/27/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A11/27/202012/31/2021
Labeler - Sonchin Biomedical Cosmetics Corp. (656155727)
Establishment
NameAddressID/FEIBusiness Operations
Sonchin Biomedical Cosmetics Corp.656155727manufacture(73662-015)

Revised: 6/2022
Document Id: e14f5e54-dc6d-5756-e053-2a95a90a205b
Set id: b5110e9d-6ced-0060-e053-2a95a90a43dc
Version: 2
Effective Time: 20220613