MEDISPRAY

Manufacturer
MEDIPLUS | K.Boeun Pharmaceutical Co.,Ltd.
Effective date
2022-04-14
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:49:13

Label at a glance#

ProductMEDISPRAY
Active ingredientOYSTER SHELL CALCIUM CARBONATE, CRUDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Calcined Weathered Sedimentary Coral Powder

INACTIVE INGREDIENT SECTION

levan, lemon flavor, water

OTC - PURPOSE SECTION

hand sanitizing tissue to help reduce bacteria on the skin

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

pull ouy wipes and sanitize hands when necessary

WARNINGS SECTION

Do not use

- in children less than 2 months of age

Do not spray directly with your eyes open. If it gets into your eyes and causes irritation, rinse thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children.

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
82622-0001-12025-01-30C16284748780-12cef2736-72ce-d83d-e063-dadaa90ab31fda67d62d-7d0b-1bbc-e053-2995a90a3c0c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82622-0001-1MEDISPRAY50 mL in 1 BOTTLELIQUID502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82622-0001MEDISPRAY (CALCINED WEATHERED SEDIMENTARY CORAL POWDER) LIQUID [MEDIPLUS]2Legacy NDC, 1 package rows20220415_da67d62d-7d0b-1bbc-e053-2995a90a3c0c.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82622-000182622-0001-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 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
dca7b2f5-6dcb-a7cb-e053-2a95a90adafdda67d62d-7d0b-1bbc-e053-2995a90a3c0c2022-04-14WarningsExact identifier
spl id: dca7b2f5-6dcb-a7cb-e053-2a95a90adafd
spl set id: da67d62d-7d0b-1bbc-e053-2995a90a3c0c

Reported adverse events (FAERS/openFDA)#

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