BEKLYN ABSOLUTE PURIFYING HAND GEL REFRESHING ALOE 180ML- titanium dioxide, hypochlorous acid gel 
MY Corp.,Ltd

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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MY Corp - Beklyn Absolute Purifying Hand Gel

titanium dioxide, hypochlorous acid

Aloe Vera Extract, Carbomer, Foeniculum Vulgare Fruit Extract, Maltitol, PEG-60, Polygonum Tinctorium Leaf Extract, Sorbitol, Triethanolamine, Water

Hand sanitizer to help reduce bacteria that potentially can cause disease. Recommended for repeated use

keep out of reach of the children

For external use only. 

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

Stop use and ask a doctor if irritation or rash occurs develop and persist for more than 72 hours.

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

for external use only

label

BEKLYN ABSOLUTE PURIFYING HAND GEL REFRESHING ALOE 180ML 
titanium dioxide, hypochlorous acid gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71544-0018
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE0.018 g  in 180 mL
HYPOCHLOROUS ACID (UNII: 712K4CDC10) (HYPOCHLOROUS ACID - UNII:712K4CDC10) HYPOCHLOROUS ACID0.0144 g  in 180 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
MALTITOL (UNII: D65DG142WK)  
POLYETHYLENE GLYCOL 3000 (UNII: SA1B764746)  
PERSICARIA TINCTORIA LEAF (UNII: FU6582QMPV)  
SORBITOL (UNII: 506T60A25R)  
TROLAMINE (UNII: 9O3K93S3TK)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71544-0018-1180 mL in 1 TUBE; Type 0: Not a Combination Product09/02/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other09/02/2020
Labeler - MY Corp.,Ltd (688202781)
Registrant - MY Corp.,Ltd (688202781)
Establishment
NameAddressID/FEIBusiness Operations
MY Corp.,Ltd688202781manufacture(71544-0018) , label(71544-0018) , pack(71544-0018)

Revised: 9/2020
Document Id: ae76149e-29ec-5ee4-e053-2995a90a7957
Set id: ae76149e-29eb-5ee4-e053-2995a90a7957
Version: 1
Effective Time: 20200904
 
MY Corp.,Ltd