BEKLYN ABSOLUTE PURIFYING HAND SANITIZING WIPES- titanium dioxide cloth

Beklyn Absolute Purifying Hand Sanitizing Wipes by

Drug Labeling and Warnings

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

Drug Details [pdf]

ACTIVE INGREDIENT

titanium dioxide

INACTIVE INGREDIENT

Foeniculum Vulgare Fruit Extract, Fragrance - Lemon, Laminaria Japonica Extract, Maltitol, PEG 60, Pinus Densiflora Extract, Polygonum Tinctoric Leaf Extract, Sorbitol, Water

PURPOSE

• Hand Santizer to help reduce bacteria on the skin.
• Recommended for repeated use.

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

• Tear open packet. Keep lid closed to prevent moisture loss
• Wet hadns throughly with prodict and allow to dry wipping.
• Discard after single use.

WARNINGS

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.

DOSAGE & ADMINISTRATION

for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BEKLYN ABSOLUTE PURIFYING HAND SANITIZING WIPES 
titanium dioxide cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71544-0013
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	0.56 g  in 30

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
FOENICULUM VULGARE FRUIT (UNII: J5W36Y5WG8)
PERSICARIA TINCTORIA LEAF (UNII: FU6582QMPV)
SORBITOL (UNII: 506T60A25R)
MALTITOL (UNII: D65DG142WK)
LAMINARIA JAPONICA (UNII: WE98HW412B)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71544-0013-1	30 in 1 PACKAGE; Type 0: Not a Combination Product	07/15/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		07/15/2020

Labeler - MY Corp.,Ltd (688202781)

Registrant - MY Corp.,Ltd (688202781)

Establishment
Name	Address	ID/FEI	Business Operations
MY Corp.,Ltd		688202781	manufacture(71544-0013) , label(71544-0013) , pack(71544-0013)