Home NDC 63083-9254-1 Creosote Combination
Product NDC 63083-9254
Requested package NDC 63083-9254-1
11-digit product format 630839254
Labeler code 63083
Product ID 63083-9254_9efdecb8-b860-4856-917e-c8b2302a817c
Type HUMAN OTC DRUG
Nonproprietary name Creosote Combination
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance ACONITUM NAPELLUS WHOLE; AMARYLLIS BELLADONNA WHOLE; ANTIMONY POTASSIUM TARTRATE; BRYONIA ALBA ROOT; CLOSTRIDIUM TETANI TOXOID ANTIGEN (FORMALDEHYDE INACTIVATED); HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED; HYOSCYAMUS NIGER; IPECAC; LOBARIA PULMONARIA; LOBELIA INFLATA WHOLE; PHOSPHORUS; SILICON DIOXIDE; WOOD CREOSOTE
Active strength 4; 4; 6; 4; 30; 30; 4; 4; 4; 4; 5; 6; 6 [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL
Pharmacologic classes Actively Acquired Immunity [PE], Inactivated Clostridium Tetani Vaccine [EPC], Tetanus Toxoid [CS], Vaccines, Inactivated [CS]
NDC exclude flag No
Listing certified through 2027-12-31
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 · 15 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 1332a3947898…d4bfe170f9cd…
Additional Listing Data#
Finished product Yes
Brand name base Creosote Combination
Brand name suffix 9254
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACONITUM NAPELLUS WHOLE 4 [hp_X]/29.5mL AMARYLLIS BELLADONNA WHOLE 4 [hp_X]/29.5mL BRYONIA ALBA ROOT 6 [hp_X]/29.5mL HYOSCYAMUS NIGER 4 [hp_X]/29.5mL IPECAC 30 [hp_X]/29.5mL LOBELIA INFLATA WHOLE 30 [hp_X]/29.5mL LOBARIA PULMONARIA 4 [hp_X]/29.5mL PHOSPHORUS 4 [hp_X]/29.5mL ANTIMONY POTASSIUM TARTRATE 4 [hp_X]/29.5mL WOOD CREOSOTE 4 [hp_X]/29.5mL SILICON DIOXIDE 5 [hp_X]/29.5mL HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED 6 [hp_X]/29.5mL CLOSTRIDIUM TETANI TOXOID ANTIGEN (FORMALDEHYDE INACTIVATED) 6 [hp_X]/29.5mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 13 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# Effective, Related label table Effective Related label 2026-01-09 R254 2026-01-09 R254 2024-01-30 R254 2024-01-30 R254
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-9254-1 Creosote Combination9254 29.5 mL in 1 BOTTLE, DROPPER LIQUID 29.5 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63083-9254 CREOSOTE COMBINATION 9254 (CREOSOTE COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220210_9248c4d5-75a5-4b52-b6b1-b2b8af8da827.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 63083-9254-1 63083925401 29.5 mL in 1 BOTTLE, DROPPER (63083-9254-1) 29.5 ml 1985-08-15 0000-00-00 No No Current