Home NDC 10893-540 Naturasil
Product NDC 10893-540
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 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 · 16 matching rows.
View current auxiliary records. · View the auxiliary file history.
Additional Listing Data#
Finished product Yes
Brand name base Naturasil
Brand name suffix Warts
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength THUJA OCCIDENTALIS LEAFY TWIG 6 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1NT28V9397 Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 10893-540-10 NaturasilWarts 10 mL in 1 BOTTLE, GLASS LIQUID 10 5 10893-540-15 NaturasilWarts 15 mL in 1 BOTTLE, GLASS LIQUID 15 5 10893-540-30 NaturasilWarts 30 mL in 1 BOTTLE, GLASS LIQUID 30 5 10893-540-50 NaturasilWarts 50 mL in 1 BOTTLE, GLASS LIQUID 50 5
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 10893-540 NATURASIL WARTS (THUJA OCCIDENTALIS) LIQUID [NATURE'S INNOVATION, INC.] 4 Current NDC, Legacy NDC, 4 package rows 20210115_a8396d10-ff5b-4f5d-a320-a46c6d788df5.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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 10893-540-10 10893054010 10 mL in 1 BOTTLE, GLASS 10 ml Historical 10893-540-15 10893054015 15 mL in 1 BOTTLE, GLASS (10893-540-15) 15 ml 2011-10-01 0000-00-00 No No Current 10893-540-30 10893054030 30 mL in 1 BOTTLE, GLASS (10893-540-30) 30 ml 2011-10-01 0000-00-00 No No Current 10893-540-50 10893054050 50 mL in 1 BOTTLE, GLASS (10893-540-50) 50 ml 2011-10-01 0000-00-00 No No Current