Home NDC 68229-100 Skin Tag Relief
Product NDC 68229-100
11-digit product format 682290100
Labeler code 68229
Product ID 68229-100_262e23fb-5ad8-bbde-e063-6394a90ab37b
Type HUMAN OTC DRUG
Nonproprietary name Thuja Occidentalis Leafy Twig
Dosage form OIL
Route TOPICAL
Labeler Quest Products, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2013-05-21
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 Skin Tag Relief
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.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 68229-100-01 Skin Tag Relief 10 mL in 1 BOTTLE, WITH APPLICATOR OIL 10 7 68229-100-02 Skin Tag Relief 1 in 1 CARTON OIL 1 7 68229-100-03 Skin Tag Relief 12.5 mL in 1 BOTTLE, WITH APPLICATOR OIL 12.5 7 68229-100-04 Skin Tag Relief 1 in 1 CARTON OIL 1 7
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 68229-100 SKIN TAG RELIEF (THUJA OCCIDENTALIS LEAFY TWIG) OIL [QUEST PRODUCTS, INC.] 7 Current NDC, Legacy NDC, 4 package rows 20241107_98fb9d4a-d0d2-425b-878b-927eebf53067.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 68229-100-01 68229010001 10 mL in 1 BOTTLE, WITH APPLICATOR 10 ml Historical 68229-100-02 68229010002 1 BOTTLE, WITH APPLICATOR in 1 CARTON (68229-100-02) / 10 mL in 1 BOTTLE, WITH APPLICATOR (68229-100-01) 2013-05-21 0000-00-00 No No Current 68229-100-03 68229010003 12.5 mL in 1 BOTTLE, WITH APPLICATOR 12.5 ml Historical 68229-100-04 68229010004 1 BOTTLE, WITH APPLICATOR in 1 CARTON (68229-100-04) / 12.5 mL in 1 BOTTLE, WITH APPLICATOR (68229-100-03) 2022-05-23 0000-00-00 No No Current