Naturasil

Product NDC
10893-430
11-digit product format
108930430
Labeler code
10893
Product ID
10893-430_6cd7cea0-5465-4704-9517-3acd5f9bb4a6
Type
HUMAN OTC DRUG
Nonproprietary name
Sulfur
Dosage form
CREAM
Route
TOPICAL
Labeler
Nature's Innovation, Inc
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2020-09-11
Substance
SULFUR
Active strength
.1 g/100mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage10893-43010893-430-02DDiscontinued by firm2026-08-17

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 1 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage10893-43010893-430-02DDiscontinued by firmexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…

Additional Listing Data#

Finished product
Yes
Brand name base
Naturasil
Brand name suffix
Mite Be Gone
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SULFUR.1 g/100mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
70FD1KFU70Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
a482f578-28df-48b0-a6ae-37350d258814Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10893-430-02NaturasilMite Be Gone60 mL in 1 JARCREAM602
10893-430-03NaturasilMite Be Gone1 in 1 BOXCREAM12
10893-430-03NaturasilMite Be Gone60 mL in 1 JARCREAM602
10893-430-04NaturasilMite Be Gone118.3 mL in 1 JARCREAM118.32
10893-430-08NaturasilMite Be Gone236.6 mL in 1 JARCREAM236.62

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10893-430NATURASIL MITE BE GONE (SULFUR) CREAM [NATURE'S INNOVATION, INC]1Current NDC, Legacy NDC, 5 package rows20201013_a482f578-28df-48b0-a6ae-37350d258814.zip

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
Naturasil Mite Be GoneSULFURNature's Innovation, Inca482f578-28df-48b0-a6ae-37350d2588142025-10-09WarningsExact identifier
ndc (product): 10893-430

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
10893-430-021089304300260 mL in 1 JAR (10893-430-02) 60 ml2020-09-110000-00-00NoNoCurrent
10893-430-03108930430031 JAR in 1 BOX (10893-430-03) / 60 mL in 1 JAR1 jar2025-10-22NoNoCurrent
10893-430-0410893043004118.3 mL in 1 JAR (10893-430-04) 118.3 ml2020-09-110000-00-00NoNoCurrent
10893-430-0810893043008236.6 mL in 1 JAR (10893-430-08) 236.6 ml2020-09-110000-00-00NoNoCurrent