Naturasil

Product NDC
10893-520
Requested package NDC
10893-520-50
11-digit product format
108930520
Labeler code
10893
Product ID
10893-520_a1a2fbe6-52e9-4041-a4ac-bed9a843db69
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]/1
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 packagepackage10893-52010893-520-50DDiscontinued by firm2026-07-31

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 Skin TagsTHUJA OCCIDENTALISNature's Innovation, Inc.e54f5257-8201-4800-9c4a-58c135978ee82025-07-25WarningsExact identifier
ndc (package): 10893-520-50
ndc (product): 10893-520
ndc11 (package): 10893052050

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
THUJA OCCIDENTALIS LEAFY TWIG6 [hp_X]/1

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
e54f5257-8201-4800-9c4a-58c135978ee8Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10893-520-10NaturasilSkin Tags1 in 1 BOTTLE, GLASSLIQUID16
10893-520-15NaturasilSkin Tags1 in 1 BOTTLE, GLASSLIQUID16
10893-520-50NaturasilSkin Tags1 in 1 BOTTLE, GLASSLIQUID16

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10893-520NATURASIL SKIN TAGS (THUJA OCCIDENTALIS) LIQUID [NATURE'S INNOVATION, INC. ]5Current NDC, Legacy NDC, 3 package rows20210115_e54f5257-8201-4800-9c4a-58c135978ee8.zip
10893-520NATURASIL SKIN TAGS (THUJA OCCIDENTALIS) LIQUID [NATURE'S INNOVATION, INC.]4Current NDC, Legacy NDC20210115_0270776f-beba-4769-9658-68f46842496c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
10893-520-50108930520501 LIQUID in 1 BOTTLE, GLASS (10893-520-50) 1 liquid2011-10-010000-00-00NoNoCurrent