FDA.reportPublic FDA data

Naturasil

Product NDC
10893-540
Requested package NDC
10893-540-50
11-digit product format
108930540
Labeler code
10893
Product ID
10893-540_70ebc7f1-7879-42e5-82c4-dbd053079ab9
Type
HUMAN OTC DRUG
Nonproprietary name
Thuja Occidentalis
Dosage form
LIQUID
Route
TOPICAL
Labeler
Nature's Innovation, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2011-10-01
Substance
THUJA OCCIDENTALIS LEAFY TWIG
Active strength
6 [hp_X]/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

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

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage10893-54010893-540-50DDiscontinued by firm2026-08-03

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Naturasil WartsTHUJA OCCIDENTALISNature's Innovation, Inc.a8396d10-ff5b-4f5d-a320-a46c6d788df52025-07-25WarningsExact identifier
ndc (package): 10893-540-50
ndc (product): 10893-540
ndc11 (package): 10893054050

Additional Listing Data#

Finished product
Yes
Brand name base
Naturasil
Brand name suffix
Warts
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
THUJA OCCIDENTALIS LEAFY TWIG6 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1NT28V9397Internal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
a8396d10-ff5b-4f5d-a320-a46c6d788df5Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10893-540-10NaturasilWarts10 mL in 1 BOTTLE, GLASSLIQUID105
10893-540-15NaturasilWarts15 mL in 1 BOTTLE, GLASSLIQUID155
10893-540-30NaturasilWarts30 mL in 1 BOTTLE, GLASSLIQUID305
10893-540-50NaturasilWarts50 mL in 1 BOTTLE, GLASSLIQUID505

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
THUJA OCCIDENTALIS LEAFY TWIGACTIVE INGREDIENT1NT28V9397NATURASIL WARTS (THUJA OCCIDENTALIS) LIQUID [NATURE'S INNOVATION, INC.]2
THUJA OCCIDENTALIS LEAFY TWIGACTIVE MOIETY1NT28V9397NATURASIL WARTS (THUJA OCCIDENTALIS) LIQUID [NATURE'S INNOVATION, INC.]2
CASTOR OILINACTIVE INGREDIENTD5340Y2I9GNATURASIL WARTS (THUJA OCCIDENTALIS) LIQUID [NATURE'S INNOVATION, INC.]2
CEDAR LEAF OILINACTIVE INGREDIENTBJ169U4NLGNATURASIL WARTS (THUJA OCCIDENTALIS) LIQUID [NATURE'S INNOVATION, INC.]2
TEA TREE OILINACTIVE INGREDIENTVIF565UC2GNATURASIL WARTS (THUJA OCCIDENTALIS) LIQUID [NATURE'S INNOVATION, INC.]2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10893-540NATURASIL WARTS (THUJA OCCIDENTALIS) LIQUID [NATURE'S INNOVATION, INC.]4Current NDC, Legacy NDC, 4 package rows20210115_a8396d10-ff5b-4f5d-a320-a46c6d788df5.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
10893-540-501089305405050 mL in 1 BOTTLE, GLASS (10893-540-50) 50 ml2011-10-010000-00-00NoNoCurrent