NDC 65734-348-00 - Fungus Relief

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
65734-348
Requested NDC
65734-348-00
Package NDCs from labels
65734-348-00, 65734-348-36
Manufacturer
Swabplus Inc.
Effective date
2015-01-28
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Fungus Relief SwabSwabplus Inc.2015-01-28HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
65734-348-362020-01-31C16284748780-19d75b9d0-2cd7-f424-e053-dadaa90a57ceFungus Relief Swab

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
65734-348-00Fungus Relief0.15 mL in 1 APPLICATORSOLUTION0.156
65734-348-36Fungus Relief36 in 1 PACKAGESOLUTION366

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
65734-348FUNGUS RELIEF (TOLNAFTATE) SOLUTION [SWABPLUS INC.]6Legacy NDC, 2 package rows20150131_3c60459f-19c3-479a-b17e-ac0cbd9dc75e.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
TOLNAFTATEACTIVE INGREDIENT06KB629TKVFUNGUS RELIEF (TOLNAFTATE) SOLUTION [SWABPLUS INC.]6
TOLNAFTATEACTIVE MOIETY06KB629TKVFUNGUS RELIEF (TOLNAFTATE) SOLUTION [SWABPLUS INC.]6
ALOE VERA LEAFINACTIVE INGREDIENTZY81Z83H0XFUNGUS RELIEF (TOLNAFTATE) SOLUTION [SWABPLUS INC.]6
BUTYLATED HYDROXYTOLUENEINACTIVE INGREDIENT1P9D0Z171KFUNGUS RELIEF (TOLNAFTATE) SOLUTION [SWABPLUS INC.]6
BUTYLENE GLYCOLINACTIVE INGREDIENT3XUS85K0RAFUNGUS RELIEF (TOLNAFTATE) SOLUTION [SWABPLUS INC.]6
DIAZOLIDINYL UREAINACTIVE INGREDIENTH5RIZ3MPW4FUNGUS RELIEF (TOLNAFTATE) SOLUTION [SWABPLUS INC.]6
DIETHYLENE GLYCOL MONOETHYL ETHERINACTIVE INGREDIENTA1A1I8X02BFUNGUS RELIEF (TOLNAFTATE) SOLUTION [SWABPLUS INC.]6
METHYLPARABENINACTIVE INGREDIENTA2I8C7HI9TFUNGUS RELIEF (TOLNAFTATE) SOLUTION [SWABPLUS INC.]6
PROPYLENE GLYCOLINACTIVE INGREDIENT6DC9Q167V3FUNGUS RELIEF (TOLNAFTATE) SOLUTION [SWABPLUS INC.]6
PROPYLPARABENINACTIVE INGREDIENTZ8IX2SC1OHFUNGUS RELIEF (TOLNAFTATE) SOLUTION [SWABPLUS INC.]6

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 24 of 24 · 466 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Miracle FootCream LemonUREA, GLYCERIN, ALOE, DISODIUM EDTAAloe Vera Korea Co.,Ltd.db525c63-29fd-2033-e053-2995a90a56b92022-03-28WarningsExact identifier
unii: ZY81Z83H0X
Flora PlusALOE, ALUMINA, ANTIMON CRUD, ARG NIT, CHELIDONIUM MAJ, GAMBOGIA, GRAPHITES, HYDRASTIS, LYCOPODIUM, SILICEANET Remediesfc1ced48-bd9f-4b3f-b786-573fba0729752021-01-21WarningsExact identifier
unii: ZY81Z83H0X
Day and Night VitalsALLIUM SAT, ALOE, ARSENICUM ALB, BERBER VULG, CALC PHOS, CEANOTHUS, CHELIDONIUM MAJ, CHOLESTERINUM, CLEMATIS ERECTA, CONDURANGO, GAMBOGIA, HAMAMELIS, KALI BROM, KALI PHOS, LYCOPODIUM, NAT CARB, PASSIFLORA, SENNA, SILICEA, SOLIDAGO, SPIGELIA ANTH, SPONGIA, VERATRUM VIRNET Remediesd5ddba51-5f0c-4b06-8f87-3cd6faf64b792021-01-19WarningsExact identifier
unii: ZY81Z83H0X
AdditoxTRIFOLIUM PRATENSE, XANTHOXYLUM FRAXINEUM, PHYTOLACCA DECANDRA, ARSENICUM ALBUM, BELLADONNA, CHELIDONIUM MAJUS, LYCOPODIUM CLAVATUM, PHOSPHORICUM ACIDUM, ASPARTAME, BENZALKONIUM CHLORIDE, FORMALINUM, METHYLENE CHLORIDE, METHYLPARABEN, PROPYLPARABEN, SODIUM BENZOATE, SODIUM CITRATE, TITANIUM DIOXIDE, ZINCUM OXYDATUMBioActive Nutritional, Inc.319ee2fe-58e3-495e-bf0d-df201f6fbb1c2018-07-18WarningsExact identifier
unii: Z8IX2SC1OH
unii: A2I8C7HI9T
Aftate Athlete Foot CreamTOLNAFTATESabel Med LLC2aa58a66-e00b-74c9-e054-00144ff88e882016-11-23WarningsExact identifier
unii: 06KB629TKV
5bc934c7-f185-4f4f-b866-26591873fbe93c60459f-19c3-479a-b17e-ac0cbd9dc75e2015-01-28WarningsExact identifier
spl id: 5bc934c7-f185-4f4f-b866-26591873fbe9
spl set id: 3c60459f-19c3-479a-b17e-ac0cbd9dc75e

Reported adverse events (FAERS/openFDA)#

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