Home NDC 63083-9238-1 Pulsatilla Combination
Product NDC 63083-9238
Requested package NDC 63083-9238-1
11-digit product format 630839238
Labeler code 63083
Product ID 63083-9238_01759f56-3b52-43df-9808-5f3b82f9a674
Type HUMAN OTC DRUG
Nonproprietary name Pulsatilla Combination
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance BRYONIA ALBA ROOT; LYCOPODIUM CLAVATUM SPORE; STRYCHNOS NUX-VOMICA SEED; PULSATILLA MONTANA WHOLE; SILVER NITRATE; CITRULLUS COLOCYNTHIS FRUIT PULP; ANTIMONY TRISULFIDE; ARSENIC TRIOXIDE; ACTIVATED CHARCOAL; BOS TAURUS COLON; GIARDIA LAMBLIA; BOS TAURUS LARGE INTESTINE; MERCURIC CHLORIDE; TRIPE
Active strength 4; 4; 4; 4; 6; 6; 8; 8; 8; 12; 12; 12; 12; 12 [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; [hp_X]/29.5mL
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [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…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Pulsatilla Combination
Brand name suffix 9238
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BRYONIA ALBA ROOT 4 [hp_X]/29.5mL LYCOPODIUM CLAVATUM SPORE 4 [hp_X]/29.5mL STRYCHNOS NUX-VOMICA SEED 4 [hp_X]/29.5mL PULSATILLA MONTANA WHOLE 4 [hp_X]/29.5mL SILVER NITRATE 6 [hp_X]/29.5mL CITRULLUS COLOCYNTHIS FRUIT PULP 6 [hp_X]/29.5mL ANTIMONY TRISULFIDE 8 [hp_X]/29.5mL ARSENIC TRIOXIDE 8 [hp_X]/29.5mL ACTIVATED CHARCOAL 8 [hp_X]/29.5mL BOS TAURUS COLON 12 [hp_X]/29.5mL GIARDIA LAMBLIA 12 [hp_X]/29.5mL BOS TAURUS LARGE INTESTINE 12 [hp_X]/29.5mL MERCURIC CHLORIDE 12 [hp_X]/29.5mL TRIPE 12 [hp_X]/29.5mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 14 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# Effective, Related label table Effective Related label 2026-01-08 R238 2026-01-08 R238 2024-01-30 R238 2024-01-30 R238
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-9238-1 Pulsatilla Combination9238 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 63083-9238 PULSATILLA COMBINATION 9238 (PULSATILLA COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220210_aee2e5f5-8171-4a1a-8ea0-5d78ec22c8a8.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 63083-9238-1 63083923801 29.5 mL in 1 BOTTLE, DROPPER (63083-9238-1) 29.5 ml 1985-08-15 0000-00-00 No No Current