MY Corp - Beklyn Absolute Purifying Hand Gel

Beklyn Absolute Purifying Hand Gel by

Drug Labeling and Warnings

Beklyn Absolute Purifying Hand Gel by is a Otc medication manufactured, distributed, or labeled by MY Corp.,Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

BEKLYN ABSOLUTE PURIFYING HAND GEL- 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

• Squeeze enough product in your palm to cover hands and rub hands together until dry.
• For children under 6 years use adult supervision
• Not recommended for infants

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

BEKLYN ABSOLUTE PURIFYING HAND GEL 
titanium dioxide, hypochlorous acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71544-0015
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	0.006 g  in 60 mL
HYPOCHLOROUS ACID (UNII: 712K4CDC10) (HYPOCHLOROUS ACID - UNII:712K4CDC10)	HYPOCHLOROUS ACID	0.0048 g  in 60 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71544-0015-1	60 mL in 1 TUBE; Type 0: Not a Combination Product	09/02/2020	09/02/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		09/02/2020	09/02/2020

Labeler - MY Corp.,Ltd (688202781)

Registrant - MY Corp.,Ltd (688202781)

Establishment
Name	Address	ID/FEI	Business Operations
MY Corp.,Ltd		688202781	manufacture(71544-0015) , label(71544-0015) , pack(71544-0015)

Revised: 9/2020

Document Id: ae7610ed-243b-2e0c-e053-2995a90a03cf

34390-5

Set id: ae6089c7-b199-ee17-e053-2a95a90ad95d

Version: 2

Effective Time: 20200904

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