Beklyn Absolute Purifying-Spray

Manufacturer
MY Corp.,Ltd
Effective date
2020-07-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:21:26

Label at a glance#

ProductBeklyn Absolute Purifying-Spray
Active ingredientTITANIUM DIOXIDE, HYPOCHLOROUS ACID
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

titanium dioxide, hypochlorous acid

INACTIVE INGREDIENT SECTION

Foeniculum Vulgare Fruit Extract, Maltitol, Polygonum Tinctorium Leaf Extract, Sorbitol, Water

OTC - PURPOSE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

  • Spray directly, from a distance of about 8 to 10 inches and rub hands together until dry.
  • For children under 6 years use adult supervision
  • Not recommended for infants

WARNINGS SECTION

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 SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71544-0001-12023-01-30C16284748780-1f386c649-ebe9-0266-e053-dadaa90a7c1aMY Corp - bekly spray 60ml

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71544-0001-1Beklyn Absolute Purifying-Spray60 mL in 1 BOTTLE, SPRAYLIQUID601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71544-0001BEKLYN ABSOLUTE PURIFYING-SPRAY (TITANIUM DIOXIDE, HYPOCHLOROUS ACID) LIQUID [MY CORP.,LTD]1Legacy NDC, 1 package rows20200715_aa75c00a-13c5-0e3e-e053-2a95a90ad321.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71544-000171544-0001-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
aa75b40c-1606-e345-e053-2995a90a036baa75c00a-13c5-0e3e-e053-2a95a90ad3212020-07-15WarningsExact identifier
spl id: aa75b40c-1606-e345-e053-2995a90a036b
spl set id: aa75c00a-13c5-0e3e-e053-2a95a90ad321

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.