FDA.reportPublic FDA data

NDC 57520-0712-2 - Loma Lux Psoriasis

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
57520-0712
Requested NDC
57520-0712-2
Package NDCs from labels
57520-0712-1, 57520-0712-2, 57520-0712-3
Manufacturer
Apotheca Company
Effective date
2011-07-05
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Loma Lux Psoriasis - Apotheca CompanyApotheca Company2011-07-05HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
57520-0712-32020-01-31C16284748780-19d75b9d0-fa09-f424-e053-dadaa90a57ceLoma Lux Psoriasis

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
57520-0712-1Loma Lux Psoriasis237 mL in 1 BOTTLELIQUID2371
57520-0712-2Loma Lux Psoriasis1 in 1 CARTONLIQUID11
57520-0712-3Loma Lux Psoriasis1 in 1 CARTONLIQUID11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
57520-0712LOMA LUX PSORIASIS (KALI BROMATUM, NATRUM SULPHURICUM, NICCOLUM SULPHURICUM, KALI SULPHURICUM, ZINCUM BROMATUM,) LIQUID [APOTHECA COMPANY]1Legacy NDC, 3 package rows20110706_06616a68-5a01-4a8f-9269-6c28825cf0a7.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
NICKEL SULFATE HEXAHYDRATEACTIVE INGREDIENTJC9WZ4FK68LOMA LUX PSORIASIS (KALI BROMATUM, NATRUM SULPHURICUM, NICCOLUM SULPHURICUM, KALI SULPHURICUM, ZINCUM BROMATUM,) LIQUID [APOTHECA COMPANY]1
POTASSIUM BROMIDEACTIVE INGREDIENTOSD78555ZMLOMA LUX PSORIASIS (KALI BROMATUM, NATRUM SULPHURICUM, NICCOLUM SULPHURICUM, KALI SULPHURICUM, ZINCUM BROMATUM,) LIQUID [APOTHECA COMPANY]1
POTASSIUM SULFATEACTIVE INGREDIENT1K573LC5TVLOMA LUX PSORIASIS (KALI BROMATUM, NATRUM SULPHURICUM, NICCOLUM SULPHURICUM, KALI SULPHURICUM, ZINCUM BROMATUM,) LIQUID [APOTHECA COMPANY]1
SODIUM BROMIDEACTIVE INGREDIENTLC1V549NOMLOMA LUX PSORIASIS (KALI BROMATUM, NATRUM SULPHURICUM, NICCOLUM SULPHURICUM, KALI SULPHURICUM, ZINCUM BROMATUM,) LIQUID [APOTHECA COMPANY]1
ZINC BROMIDEACTIVE INGREDIENTOO7ZBU9703LOMA LUX PSORIASIS (KALI BROMATUM, NATRUM SULPHURICUM, NICCOLUM SULPHURICUM, KALI SULPHURICUM, ZINCUM BROMATUM,) LIQUID [APOTHECA COMPANY]1
NICKELACTIVE MOIETY7OV03QG267LOMA LUX PSORIASIS (KALI BROMATUM, NATRUM SULPHURICUM, NICCOLUM SULPHURICUM, KALI SULPHURICUM, ZINCUM BROMATUM,) LIQUID [APOTHECA COMPANY]1
POTASSIUM CATIONACTIVE MOIETY295O53K152LOMA LUX PSORIASIS (KALI BROMATUM, NATRUM SULPHURICUM, NICCOLUM SULPHURICUM, KALI SULPHURICUM, ZINCUM BROMATUM,) LIQUID [APOTHECA COMPANY]1
SODIUM CATIONACTIVE MOIETYLYR4M0NH37LOMA LUX PSORIASIS (KALI BROMATUM, NATRUM SULPHURICUM, NICCOLUM SULPHURICUM, KALI SULPHURICUM, ZINCUM BROMATUM,) LIQUID [APOTHECA COMPANY]1
ZINC CATIONACTIVE MOIETY13S1S8SF37LOMA LUX PSORIASIS (KALI BROMATUM, NATRUM SULPHURICUM, NICCOLUM SULPHURICUM, KALI SULPHURICUM, ZINCUM BROMATUM,) LIQUID [APOTHECA COMPANY]1
ALCOHOLINACTIVE INGREDIENT3K9958V90MLOMA LUX PSORIASIS (KALI BROMATUM, NATRUM SULPHURICUM, NICCOLUM SULPHURICUM, KALI SULPHURICUM, ZINCUM BROMATUM,) LIQUID [APOTHECA COMPANY]1
METHYLPARABENINACTIVE INGREDIENTA2I8C7HI9TLOMA LUX PSORIASIS (KALI BROMATUM, NATRUM SULPHURICUM, NICCOLUM SULPHURICUM, KALI SULPHURICUM, ZINCUM BROMATUM,) LIQUID [APOTHECA COMPANY]1
PROPYLPARABENINACTIVE INGREDIENTZ8IX2SC1OHLOMA LUX PSORIASIS (KALI BROMATUM, NATRUM SULPHURICUM, NICCOLUM SULPHURICUM, KALI SULPHURICUM, ZINCUM BROMATUM,) LIQUID [APOTHECA COMPANY]1
WATERINACTIVE INGREDIENT059QF0KO0RLOMA LUX PSORIASIS (KALI BROMATUM, NATRUM SULPHURICUM, NICCOLUM SULPHURICUM, KALI SULPHURICUM, ZINCUM BROMATUM,) LIQUID [APOTHECA COMPANY]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 7 of 159 · 3,176 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
SprinJeneALCOHOLHealth and Natural Beauty USA Corp1853f023-f4db-4cd8-a4df-a439bc306cc32026-08-13WarningsExact identifier
unii: 3K9958V90M
FRESH FEELS HAND SANITIZER MIST WATERMELON POP SCENTETHYL ALCOHOLAmber Glow Cosmetics Limited3fea32bb-98ec-4dc6-97d3-c77d8e476c042026-08-13WarningsExact identifier
unii: 3K9958V90M
WhiskCare 373ALCOHOLWhisk Products, Inc.57d5cd5d-8597-ce66-e063-6394a90a00472026-08-12WarningsExact identifier
unii: 3K9958V90M
ZoviroALCOHOLZoviro, LLC9c8ca084-8aef-4616-8d51-aaff3eb253432026-08-12WarningsExact identifier
unii: 3K9958V90M
Aire-Master Foaming Hand Sanitizer Fragrance FreeALCOHOLWhisk Products, Inc.56a8f08e-7683-d155-e063-6394a90ac77b2026-08-11WarningsExact identifier
unii: 3K9958V90M
Ethyl alcoholETHYL ALCOHOLStrategic Sourcing Services LLC4fec6f1f-0249-423f-bd3c-427aa6924c6f2026-08-10Warnings, Adverse reactionsExact identifier
unii: 3K9958V90M
MagiCare Premium Hand Sanitizing WipesALCOHOLMAGICARE TECH CORP3113dd38-257e-4b30-a611-1f259d1e3d1b2026-08-10WarningsExact identifier
unii: 3K9958V90M
Sodium Sulfate, Potassium Sulfate and Magnesium SulfateSODIUM SULFATE, POTASSIUM SULFATE AND MAGNESIUM SULFATEAscend Laboratories, LLC2106d1aa-086e-4248-9a3d-ec138d492cf32026-08-08Warnings, Adverse reactionsExact identifier
unii: 1K573LC5TV
B-Pure Moisturizing Hand Sanitizer, Orchid Vanilla ScentedALCOHOLFourstar Group USA, Inc.cca1b0ff-f8bd-4440-939e-de3fb7920c2d2026-08-07WarningsExact identifier
unii: 3K9958V90M
B-Pure Moisturizing Hand Sanitizer Raspberry White Tea ScentedALCOHOLFourstar Group USA, Inc.c673389a-7154-440f-a1d4-60fe7bcf54f22026-08-07WarningsExact identifier
unii: 3K9958V90M
CVS Beauty Hydrating Hand Sanitizer SANDALWOOD MUSKETHYL ALCOHOLCVS Pharmacy, Inc.60128fc3-b127-44ee-9e9b-384d322d213a2026-08-07WarningsExact identifier
unii: 3K9958V90M
CVS Beauty Hydrating Hand Sanitizer Sea Salt and LavenderETHYL ALCOHOLCVS Pharmacy, Inc.6c160826-ad98-4390-a07b-c92a2ae5b1812026-08-07WarningsExact identifier
unii: 3K9958V90M
Sterile WaterWATERCardinal Health 107, LLC48d75a7c-8329-48a8-bea0-a8c144ddf6372026-08-07Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Hydrating Hand Sanitizer ROSEWATER SPRITZALCOHOL 75%Guangzhou Ailizhuangsi Cosmetics Co., Ltd.585cb4fa-6016-1550-e063-6294a90a514d2026-08-06WarningsExact identifier
unii: 3K9958V90M
ALCOHOL WIPEALCOHOL CLOTHJINHUA JINGDI MEDICAL SUPPLIES CO.,LTD585daf42-ec83-d222-e063-6294a90a83702026-08-06WarningsExact identifier
unii: 3K9958V90M
Hydrating Hand Sanitizer PASSION MANGO SPLASHALCOHOL 75%Guangzhou Ailizhuangsi Cosmetics Co., Ltd.585df6ce-4625-d5d2-e063-6394a90a7fcb2026-08-06WarningsExact identifier
unii: 3K9958V90M
Hydrating Hand Sanitizer LILY SPRINGSALCOHOL 75%Guangzhou Ailizhuangsi Cosmetics Co., Ltd.585e0c24-7f5f-4ba7-e063-6294a90a75972026-08-06WarningsExact identifier
unii: 3K9958V90M
Hydrating Hand Sanitizer WATERMELON POPALCOHOL 75%Guangzhou Ailizhuangsi Cosmetics Co., Ltd.585e3ced-fa45-8576-e063-6294a90af50f2026-08-06WarningsExact identifier
unii: 3K9958V90M
Hydrating Hand Sanitizer ALOE BREEZEALCOHOL 75%Guangzhou Ailizhuangsi Cosmetics Co., Ltd.585e647c-2904-2d3f-e063-6394a90a2b792026-08-06WarningsExact identifier
unii: 3K9958V90M
Hydrating Hand Sanitizer LAVENDER DREAMALCOHOL 75%Guangzhou Ailizhuangsi Cosmetics Co., Ltd.585e8222-fad5-4409-e063-6394a90a9c602026-08-06WarningsExact identifier
unii: 3K9958V90M

Reported adverse events (FAERS/openFDA)#

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