Elrose Labs

Manufacturer
Elroselabs Inc.
Effective date
2015-12-17
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:07:01

Label at a glance#

ProductElrose Labs
Active ingredientSILICON DIOXIDE, OYSTER SHELL CALCIUM CARBONATE, CRUDE, SODIUM CHLORIDE, POTASSIUM CHLORIDE, POTASSIUM BROMIDE
Label structure8 sections

Label contents#

Full prescribing information#

WARNINGS SECTION

For external use only. do not use on large areas, on wounds, punctured skin, in eyes, animal bites or burns. Stop use if rash or allergic reaction occurs/ condition worsens.

OTC - ACTIVE INGREDIENT SECTION

SILICEA

CALCAREA CARBONICA

THUJA  OIL

NATRUM MURIATICUM

KALI BROMATUM

SULPHAR

KALI MURIATICUM

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed induce vomit. Get medical help or contact a poison control center right away.

OTC - PURPOSE SECTION

MCV Relief

DOSAGE & ADMINISTRATION SECTION

Clean infected skin area.Apply a small amount(equal to lesion size) on each lesion. Gently rub in circular motion leaving thin cream layer.Repeat treatment 2 to 3 times daily. Let dry for 3 minutes.

INDICATIONS & USAGE SECTION

Molluscum Contagiosum Lesion Relief

INACTIVE INGREDIENT SECTION

Croton Lechleri
Emulsifying Wax NF
Polysorbate 60 
Magnesium Sulfate 
Vegetable Glycerine
Zinc Oxide
Dimethyl Isosorbide 
Tea Tree Oil
Colve Oil
Wintergreen Oil
Oragano Oil
Lemon Balm Oil 
Cedarwood Oil
Niaouli Oil
Eucalyptus Leaf  Oil
Coconut Oil

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70223-001-062020-01-31C16284748780-19d75b9d0-abdc-f424-e053-dadaa90a57ce9cfea924-ca0b-46a1-b1e0-3afaf2d04850

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70223-001-06Elrose Labs28.3 mg in 1 TUBECREAM28.33

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70223-001ELROSE LABS (CONZEROL) CREAM [ELROSELABS INC.]3Legacy NDC, 1 package rows20151218_9cfea924-ca0b-46a1-b1e0-3afaf2d04850.zip

Products#

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

DailyMed product names page 1 of 1 · 27 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70223-00170223-001-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 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
9032434c-247f-4875-bc69-44a7cde915289cfea924-ca0b-46a1-b1e0-3afaf2d048502015-12-17WarningsExact identifier
spl id: 9032434c-247f-4875-bc69-44a7cde91528
spl set id: 9cfea924-ca0b-46a1-b1e0-3afaf2d04850

Reported adverse events (FAERS/openFDA)#

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