NARO COMO

Manufacturer
NARO Global Inc.
Effective date
2021-05-29
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:40:37

Label at a glance#

ProductNARO COMO
Active ingredientPOTASSIUM CARBONATE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

potassium carbonate

INACTIVE INGREDIENT SECTION

ε-Polylysine.Dextrin.1,2-Propanediol.Citric Acid.Tea Catechin. Hydroxypropylmethyl Cellulose.Distilled water.

OTC - PURPOSE SECTION

Sanitizer to help decrease bacteria on skin

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

Spray on skin as needed

WARNINGS SECTION

For external use only.

When using this product

Avoid contact with eyes. Discontinue use if signs of irritation or rashes appear.

Keep out of reach of children.

Store at room temperature.

DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label2label2label1label1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81936-0001-12023-01-30C16284748780-1f386c649-bff6-0266-e053-dadaa90a7c1ac3821713-2def-da12-e053-2a95a90a9ec5
81936-0001-22023-01-30C16284748780-1f386c649-bff6-0266-e053-dadaa90a7c1ac3821713-2def-da12-e053-2a95a90a9ec5

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81936-0001-1NARO COMO100 mL in 1 BOTTLELIQUID1002
81936-0001-2NARO COMO500 mL in 1 BOTTLELIQUID5002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81936-0001NARO COMO (POTASSIUM CARBONATE) LIQUID [NARO GLOBAL INC.]2Legacy NDC, 2 package rows20210530_c3821713-2def-da12-e053-2a95a90a9ec5.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
81936-000181936-0001-1, 81936-0001-2

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
c383148c-d90d-9011-e053-2a95a90a1f6ec3821713-2def-da12-e053-2a95a90a9ec52021-05-29WarningsExact identifier
spl id: c383148c-d90d-9011-e053-2a95a90a1f6e
spl set id: c3821713-2def-da12-e053-2a95a90a9ec5

Reported adverse events (FAERS/openFDA)#

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