Home NDC 0363-3100 Walgreens Skin Tag Treatment
Product NDC 0363-3100
11-digit product format 003633100
Labeler code 0363
Product ID 0363-3100_09056983-cf95-4f82-e063-6294a90a858e
Type HUMAN OTC DRUG
Nonproprietary name Thuja Occidentalis
Dosage form LIQUID
Route TOPICAL
Labeler Walgreens
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2023-04-30
Substance THUJA OCCIDENTALIS LEAFY TWIG
Active strength 6 [hp_X]/10mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Walgreens Skin Tag Treatment
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength THUJA OCCIDENTALIS LEAFY TWIG 6 [hp_X]/10mL
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 0363-3100-10 Walgreens Skin Tag Treatment 10 mL in 1 BOTTLE, GLASS LIQUID 10 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0363-3100 WALGREENS SKIN TAG TREATMENT (THUJA OCCIDENTALIS) LIQUID [WALGREENS] 3 Current NDC, 1 package rows 20231102_d9d76497-09b7-6979-e053-2a95a90a21fe.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 Sample Exclude flag Status 0363-3100-10 00363310010 10 mL in 1 BOTTLE, GLASS (0363-3100-10) 10 ml 2023-04-30 No No Current