FDA.reportPublic FDA data

NDC 53634-010-01 - Malin and Goetz Acne Treatment

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
53634-010
Requested NDC
53634-010-01
Package NDCs from labels
53634-010-01, 53634-010-02
Manufacturer
Malin and Goetz Inc
Effective date
2026-10-06
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Malin and Goetz Acne Treatment - Malin and Goetz IncMalin and Goetz Inc2026-10-06HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
EffectiveRelated label
2024-10-30Acne treatment Nighttime
2024-10-30Acne treatment Nighttime
2024-01-30Acne treatment Nighttime
2024-01-30Acne treatment Nighttime

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53634-010-01Malin and GoetzAcne Treatment14.75 mL in 1 JARCREAM14.757
53634-010-02Malin and GoetzAcne Treatment1 in 1 CARTONCREAM17

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
53634-010MALIN AND GOETZ ACNE TREATMENT (SULFUR) CREAM [MALIN AND GOETZ INC]6Current NDC, Legacy NDC, 2 package rows20241101_47390813-6bc9-44f4-b72a-d399d2c0de27.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
SULFURACTIVE INGREDIENT70FD1KFU70MALIN AND GOETZ ACNE TREATMENT (SULFUR,SALICYLIC ACID) CREAM [MALIN AND GOETZ INC]1
SULFURACTIVE MOIETY70FD1KFU70MALIN AND GOETZ ACNE TREATMENT (SULFUR,SALICYLIC ACID) CREAM [MALIN AND GOETZ INC]1
CAMPHOR (SYNTHETIC)INACTIVE INGREDIENT5TJD82A1ETMALIN AND GOETZ ACNE TREATMENT (SULFUR,SALICYLIC ACID) CREAM [MALIN AND GOETZ INC]1
ISOPROPYL ALCOHOLINACTIVE INGREDIENTND2M416302MALIN AND GOETZ ACNE TREATMENT (SULFUR,SALICYLIC ACID) CREAM [MALIN AND GOETZ INC]1
MAGNESIUM ALUMINUM SILICATEINACTIVE INGREDIENT6M3P64V0NCMALIN AND GOETZ ACNE TREATMENT (SULFUR,SALICYLIC ACID) CREAM [MALIN AND GOETZ INC]1
SALICYLIC ACIDINACTIVE INGREDIENTO414PZ4LPZMALIN AND GOETZ ACNE TREATMENT (SULFUR,SALICYLIC ACID) CREAM [MALIN AND GOETZ INC]1
WATERINACTIVE INGREDIENT059QF0KO0RMALIN AND GOETZ ACNE TREATMENT (SULFUR,SALICYLIC ACID) CREAM [MALIN AND GOETZ INC]1
ZINC OXIDEINACTIVE INGREDIENTSOI2LOH54ZMALIN AND GOETZ ACNE TREATMENT (SULFUR,SALICYLIC ACID) CREAM [MALIN AND GOETZ INC]1

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 78 of 380 · 7,586 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Youmi Alcohol Prep Pad 70 Isopropyl AlcoholISOPROPYL ALCOHOLPT YOUMI MEDIKA INDUSTRIe3b1a576-a8eb-44bf-8f9c-a49a44a894e82026-02-09WarningsExact identifier
unii: ND2M416302
SERYNTH WART REMOVAL SystemSALICYLIC ACID 17% WART REMOVAL SYSTEMJiangxi Yudexi Pharmaceutical Co., LTD4a6ff078-3ae6-39f5-e063-6394a90a2f102026-02-09WarningsExact identifier
unii: O414PZ4LPZ
EVERLIT CARE PRODUCTS PREP PADISOPROPYL ALCOHOLEVERLIT GLOBAL INC.77a60360-8bb5-43e9-b7e4-f71d2d488c442026-02-09WarningsExact identifier
unii: ND2M416302
Everlit Care Products Sting ReliefISOPROPYL ALCOHOLEVERLIT GLOBAL INC.adfab206-b7de-4f6a-a864-edd946ea743d2026-02-09WarningsExact identifier
unii: ND2M416302
Dermveda JOCK ITCHSULPHUR, CURCUMA LONGACelcius Corp.bb9c3941-a778-49ba-b58c-75ab5b93b3d02026-02-09WarningsExact identifier
unii: 70FD1KFU70
dermveda PSORIASIS AND SEBORRHEIC DERMATITISSULFUR, CURCUMA LONGACelcius Corp.a05c1e45-ca2f-49a1-a3f9-32dc51278fb62026-02-09WarningsExact identifier
unii: 70FD1KFU70
dermveda SCABIES ITCH RELIEF SERUMOLIVE EXTRACT, SULFURCelcius Corp.86a8bffd-81a8-4f22-89b6-e51158f336db2026-02-09WarningsExact identifier
unii: 70FD1KFU70
Flobow WART REMOVERSALICYLIC ACID 17% WART REMOVERJiangxi Yudexi Pharmaceutical Co., LTD4a4a095d-7de4-de57-e063-6394a90a8a322026-02-08WarningsExact identifier
unii: O414PZ4LPZ
Flobow TAG WART REMOVERSALICYLIC ACID 17% TAG WART REMOVERJiangxi Yudexi Pharmaceutical Co., LTD4a4a26a9-d4a1-02e2-e063-6294a90a8f872026-02-08WarningsExact identifier
unii: O414PZ4LPZ
DERMFREE WART REMOVERSALICYLIC ACID 1% WART REMOVERJiangxi Yudexi Pharmaceutical Co., LTD4a5adf1c-a515-2094-e063-6294a90aa32b2026-02-08WarningsExact identifier
unii: O414PZ4LPZ
AlcoholISOPROPYL ALCOHOLA-S Medication Solutions6b8834be-0235-4f7c-8d52-c2f6aa2d30492026-02-08WarningsExact identifier
unii: ND2M416302
Herbal Knee PatchHERBAL KNEE PATCHHenan Kangdi Medical Devices Co., Ltd2a009059-b515-8214-e063-6294a90a4ed32026-02-07WarningsExact identifier
unii: 5TJD82A1ET
RushCure Wart Removal SerumSALICYLIC ACID 17% WART REMOVAL SERUMJiangxi Yudexi Pharmaceutical Co., LTD4a478898-db77-49de-e063-6294a90a5dbb2026-02-07WarningsExact identifier
unii: O414PZ4LPZ
dermveda JOCK ITCHOLIVE EXTRACT, SULFURCelcius Corp.252ed439-0e4c-419f-8b34-d1b52da8464f2026-02-06WarningsExact identifier
unii: 70FD1KFU70
NUDESCREEN DEWY ILLUMINATING GLOW SPF 30 - Goddess GlowZINC OXIDE SUNSCREENBentley Laboratories, LLCbb86322d-ff30-4a54-97b5-1be2750671462026-02-06WarningsExact identifier
unii: SOI2LOH54Z
Acne CleanserBENZOYL PEROXIDEWalmart, Inc.04514cbb-6041-4bd5-9ab9-31312b0d8f192026-02-06Warnings, Adverse reactionsExact identifier
application number: M006
Salicylic acidSALICYLIC ACIDTopco Associates LLC4a28800d-14ef-d841-e063-6394a90a692b2026-02-06Warnings, Adverse reactionsExact identifier
application number: M006
unii: O414PZ4LPZ
Jorvinl WART AND CORN REMOVERSALICYLIC ACID 40%Guangzhou Huixue Biotechnology Co., Ltd.4a299d62-ad4a-57c8-e063-6294a90acf612026-02-06WarningsExact identifier
unii: O414PZ4LPZ
Flyleaf WART REMOVERSALICYLIC ACID 20%Guangzhou Huixue Biotechnology Co., Ltd.4a29e0f1-0ff3-f782-e063-6294a90a01ea2026-02-06WarningsExact identifier
unii: O414PZ4LPZ
Hampton Sun SPF 50 MineralZINC OXIDE 19.5% TITANIUM DIOXIDE 4.00%S&C Hampton Sun LLCd6c33436-042e-44e8-8b55-98be6e2468792026-02-06WarningsExact identifier
unii: SOI2LOH54Z

Reported adverse events (FAERS/openFDA)#

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