FDA.reportPublic FDA data

AnubisMed

Manufacturer
ANUBIS COSMETICS SL | GDC OF FLORIDA IMPORTS, INC.
Effective date
2023-09-05
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:56:05

Label at a glance#

ProductAnubisMed
Active ingredientIMIDUREA, ALOE VERA LEAF, WATER
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Skin Neutralizer ingredientsSkin Neutralizer ingredients

INDICATIONS & USAGE SECTION

Skin Neutralizer indicationsSkin Neutralizer indications

OTC - DO NOT USE SECTION

Skin Neutralizer do not useSkin Neutralizer do not use

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Skin Neutralizer keepSkin Neutralizer keep

DOSAGE & ADMINISTRATION SECTION

Skin Neutralizer dosageSkin Neutralizer dosage

WARNINGS SECTION

Skin Neutralizer warningsSkin Neutralizer warnings

INACTIVE INGREDIENT SECTION

Skin Neutralizer ingredient listSkin Neutralizer ingredient list

OTC - PURPOSE SECTION

Skin Neutralizer purposeSkin Neutralizer purpose

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Skin Neutralizer displaySkin Neutralizer display

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
IMIDUREA Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83021-400-50AnubisMed50 mL in 1 BOTTLE, SPRAYLIQUID502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83021-400ANUBISMED (SODIUM BICARBONATE, ALOE BARBADENSIS LEAF JUICE, IMIDAZOLIDINYL UREA) LIQUID [ANUBIS COSMETICS SL]2Current NDC, Legacy NDC, 1 package rows20230906_ebf4b3ab-34e1-185a-e053-2a95a90ace3a.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83021-40083021-400-50

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
SODIUM BICARBONATE8MDF5V39QOIACT
IMIDUREAM629807ATLACTIB
SODIUM HYDROXIDE55X04QC32IIACT
SODIUM BENZOATEOJ245FE5EUIACT
ALOE VERA LEAFZY81Z83H0XACTIB
POTASSIUM SORBATE1VPU26JZZ4IACT
WATER059QF0KO0RACTIB

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
AnubisMedSODIUM BICARBONATE, ALOE BARBADENSIS LEAF JUICE, IMIDAZOLIDINYL UREAANUBIS COSMETICS SLebf4b3ab-34e1-185a-e053-2a95a90ace3a2023-09-05WarningsExact identifier
ndc (package): 83021-400-50
ndc (product): 83021-400
ndc11 (package): 83021040050
spl id: 049fe4c2-996a-198f-e063-6294a90a40b9
spl set id: ebf4b3ab-34e1-185a-e053-2a95a90ace3a

Reported adverse events (FAERS/openFDA)#

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