Home NDC 63083-4017 Allergy Nosode
Product NDC 63083-4017
11-digit product format 630834017
Labeler code 63083
Product ID 63083-4017_8f6adf24-31cc-4860-b955-0076730f68ba
Type HUMAN OTC DRUG
Nonproprietary name Allergy Nosode
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance CALCIUM SULFIDE; FRAXINUS LATIFOLIA WHOLE; GUAIAC; HISTAMINE; HOUSE DUST; LUFFA OPERCULATA FRUIT; MEDICAGO SATIVA WHOLE; POTASSIUM DICHROMATE; SILICON DIOXIDE; STACHYBOTRYS CHARTARUM; TARAXACUM OFFICINALE
Active strength 12; 12; 6; 12; 12; 6; 12; 30; 12; 12; 12 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
Pharmacologic classes Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Fungal Proteins [CS], House Dust [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], Non-Standardized Fungal Allergenic Extract [EPC], Non-Standardized House Dust Allergenic Extract [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes openFDA label cross-check# Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report.
Warnings cross-check# openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
warnings WARNINGS If symptoms do not improve or are accompanied by a fever, consult a doctor. Keep out of the reach of children. In case of overdose, get medical help or contact a poison control center right away. If pregnant or breastfeeding, ask a healthcare professional before use. Keep out of the reach of children. If pregnant or breastfeeding, ask a healthcare professional before use.
Additional Listing Data#
Finished product Yes
Brand name base Allergy Nosode
Brand name suffix 4017
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HOUSE DUST 12 [hp_X]/59mL STACHYBOTRYS CHARTARUM 12 [hp_X]/59mL MEDICAGO SATIVA WHOLE 6 [hp_X]/59mL FRAXINUS LATIFOLIA WHOLE 12 [hp_X]/59mL TARAXACUM OFFICINALE 12 [hp_X]/59mL POTASSIUM DICHROMATE 6 [hp_X]/59mL CALCIUM SULFIDE 12 [hp_X]/59mL HISTAMINE 30 [hp_X]/59mL SILICON DIOXIDE 12 [hp_X]/59mL GUAIAC 12 [hp_X]/59mL LUFFA OPERCULATA FRUIT 12 [hp_X]/59mL
Harmonized Identifiers# Field, Values table Field Values Unii EYO007VX98, HJ4L70T1ZP, DJO934BRBD, 024W88F557, 39981FM375, T4423S18FM, 1MBW07J51Q, 820484N8I3, ETJ7Z6XBU4, 03C8A0DFJ8, C4MO6809HU
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-4017-2 Allergy Nosode4017 59 mL in 1 BOTTLE, DROPPER LIQUID 59 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63083-4017 ALLERGY NOSODE 4017 (ALLERGY NOSODE) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220301_da9145a5-42e9-4dba-9d11-195848e628a4.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 63083-4017-2 63083401702 59 mL in 1 BOTTLE, DROPPER (63083-4017-2) 59 ml 1985-08-15 0000-00-00 No No Current