Anti-Fungal Buttery Balm

Manufacturer
Derma Care Research Labs, LLC
Effective date
2019-05-06
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-02 00:24:36

Label at a glance#

ProductAnti-Fungal Buttery Balm Lady Bits
Active ingredientMICONAZOLE NITRATE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Miconazole Nitrate 2%

OTC - PURPOSE SECTION

Antifungal

DOSAGE & ADMINISTRATION SECTION

Cures most tinea cruris "jock itch" and tinea corporis "ring worm". Soothes itching, burning, cracking.

WARNINGS SECTION

For external use only.

Avoid contact with eyes. Do not use on children under 2 years of age unless directed by a doctor.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

INDICATIONS & USAGE SECTION

Clean the affected area thoroughly. Apply a thin layer of the product over affected area twice daily (morning and night) or as directed by a doctor. If irritation occurs or if there is no improvement within 4 weeks, discontinue use and consult a doctor.

INACTIVE INGREDIENT SECTION

aloe barbadensis leaf extract, althaea officinalis root extract, beeswax, butyrospermum park ii (shea) butter, calendula officinalis flower extract, cocos nucifera (coconut) oil, cucumis melo (melon) fruit extract, dipteryx odorata seed extract, glycerin, hydrogenated vegetable oil, olea europaea (olive) fruit oil, pimpinella anisum (anise) fruit extract, ricinus communis (castor) seed oil, theobroma cacao (cocoa) extract, triethyl citrate, vanilla planifolia fruit extract, water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CartonCarton

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72839-13372839-133-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 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.

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
f28c668a-36ae-6a39-e053-2995a90a822e87c465cd-5650-dd51-e053-2a95a90ae4fe2023-01-18WarningsExact identifier
spl set id: 87c465cd-5650-dd51-e053-2a95a90ae4fe

Reported adverse events (FAERS/openFDA)#

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