Home NDC 81825-0007 Allergy
Product NDC 81825-0007
11-digit product format 818250007
Labeler code 81825
Product ID 81825-0007_dda1ff79-ce5d-47c0-99e6-0b77f3defed7
Type HUMAN OTC DRUG
Nonproprietary name Allium Cepa, Ambrosia, Arsenicum Alb, Carbo Veg, Euphrasia, Nux Vom, Phosphorus, Pulsatilla, Sulphur, Solidago
Dosage form LIQUID
Route ORAL
Labeler Zorex International
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2022-02-16
Substance ACTIVATED CHARCOAL; AMBROSIA ARTEMISIIFOLIA WHOLE; EUPHRASIA STRICTA; ONION; PHOSPHORUS; PULSATILLA VULGARIS WHOLE; SOLIDAGO VIRGAUREA FLOWERING TOP; STRYCHNOS NUX-VOMICA SEED; SULFUR
Active strength 30; 30; 30; 30; 30; 30; 30; 30; 30 [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL
Pharmacologic classes Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS], Vegetable Proteins [CS]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes 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 Allergy
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ONION 30 [hp_C]/mL AMBROSIA ARTEMISIIFOLIA WHOLE 30 [hp_C]/mL ACTIVATED CHARCOAL 30 [hp_C]/mL EUPHRASIA STRICTA 30 [hp_C]/mL STRYCHNOS NUX-VOMICA SEED 30 [hp_C]/mL PHOSPHORUS 30 [hp_C]/mL PULSATILLA VULGARIS WHOLE 30 [hp_C]/mL SULFUR 30 [hp_C]/mL SOLIDAGO VIRGAUREA FLOWERING TOP 30 [hp_C]/mL
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 Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 81825-0007-1 Allergy 30 mL in 1 BOTTLE, DROPPER LIQUID 30 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 81825-0007 ALLERGY (ALLIUM CEPA, AMBROSIA, ARSENICUM ALB, CARBO VEG, EUPHRASIA, NUX VOM, PHOSPHORUS, PULSATILLA, SULPHUR, SOLIDAGO) LIQUID [ZOREX INTERNATIONAL] 1 Current NDC, 1 package rows 20230420_4718c012-b90d-4d7a-a97c-1abec1fd3834.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.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Allergy ALLIUM CEPA, AMBROSIA, ARSENICUM ALB, CARBO VEG, EUPHRASIA, NUX VOM, PHOSPHORUS, PULSATILLA, SULPHUR, SOLIDAGO Zorex International 4718c012-b90d-4d7a-a97c-1abec1fd3834 2018-12-21 Warnings Exact identifier ndc (product): 81825-0007
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 81825-0007-1 81825000701 30 mL in 1 BOTTLE, DROPPER (81825-0007-1) 30 ml 2022-02-16 No No Current