Home NDC 63083-9261-1 Pollinosis Combination
Product NDC 63083-9261
Requested package NDC 63083-9261-1
11-digit product format 630839261
Labeler code 63083
Product ID 63083-9261_e46a0d35-ede2-4299-95da-4b02d57ce817
Type HUMAN OTC DRUG
Nonproprietary name Pollinosis Combination
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance SYMPLOCARPUS FOETIDUS ROOT; ARSENIC TRIOXIDE; EUPHRASIA STRICTA; STRYCHNOS IGNATII SEED; POTASSIUM PHOSPHATE, UNSPECIFIED FORM; LYCOPODIUM CLAVATUM SPORE; SANGUINARIA CANADENSIS ROOT; SULFUR; HISTAMINE DIHYDROCHLORIDE
Active strength 5; 6; 6; 6; 6; 6; 6; 6; 9 [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
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 Pollinosis Combination
Brand name suffix 9261
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SYMPLOCARPUS FOETIDUS ROOT 5 [hp_X]/29.5mL ARSENIC TRIOXIDE 6 [hp_X]/29.5mL EUPHRASIA STRICTA 6 [hp_X]/29.5mL STRYCHNOS IGNATII SEED 6 [hp_X]/29.5mL POTASSIUM PHOSPHATE, UNSPECIFIED FORM 6 [hp_X]/29.5mL LYCOPODIUM CLAVATUM SPORE 6 [hp_X]/29.5mL SANGUINARIA CANADENSIS ROOT 6 [hp_X]/29.5mL SULFUR 6 [hp_X]/29.5mL HISTAMINE DIHYDROCHLORIDE 9 [hp_X]/29.5mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 9 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 2026-01-09 R261 2026-01-09 R261 2024-01-30 R261 2024-01-30 R261
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-9261-1 Pollinosis Combination9261 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 63083-9261 POLLINOSIS COMBINATION 9261 (POLLINOSIS COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220210_2a4336d2-dcaa-4a15-95e5-b76c5646825a.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 63083-9261-1 63083926101 29.5 mL in 1 BOTTLE, DROPPER (63083-9261-1) 29.5 ml 1985-08-15 0000-00-00 No No Current