Home NDC 43406-0587 ALLERGY ATLANTIC MOLD MIX
Product NDC 43406-0587
11-digit product format 434060587
Labeler code 43406
Product ID 43406-0587_e1267a37-7517-45f6-aaf8-0b490255e8a4
Type HUMAN OTC DRUG
Nonproprietary name Alternaria Alternata, Aspergillus Fumigatus, Botrytis Cinerea, Rhizopus Stolonifer, Ustilago Maydis
Dosage form LIQUID
Route ORAL
Labeler Natural Creations, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2007-05-29
Substance ALTERNARIA ALTERNATA; ASPERGILLUS FUMIGATUS; BOTRYTIS CINEREA; RHIZOPUS STOLONIFER; USTILAGO MAYDIS
Active strength 8; 8; 8; 8; 8 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classes Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Fungal Proteins [CS], Fungal Proteins [CS], Fungal Proteins [CS], Fungal Proteins [CS], Fungal Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], Increased IgG Production [PE], Increased IgG Production [PE], Non-Standardized Fungal Allergenic Extract [EPC], Non-Standardized Fungal Allergenic Extract [EPC], Non-Standardized Fungal Allergenic Extract [EPC], Non-Standardized Fungal Allergenic Extract [EPC], Non-Standardized Fungal Allergenic Extract [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base ALLERGY ATLANTIC MOLD MIX
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALTERNARIA ALTERNATA 8 [hp_X]/mL ASPERGILLUS FUMIGATUS 8 [hp_X]/mL BOTRYTIS CINEREA 8 [hp_X]/mL RHIZOPUS STOLONIFER 8 [hp_X]/mL USTILAGO MAYDIS 8 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 5 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 43406-0587-1 ALLERGY ATLANTIC MOLD MIX 30 mL in 1 BOTTLE, DROPPER LIQUID 30 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 43406-0587 ALLERGY ATLANTIC MOLD MIX (ALTERNARIA ALTERNATA, ASPERGILLUS FUMIGATUS, BOTRYTIS CINEREA, RHIZOPUS STOLONIFER, USTILAGO MAYDIS) LIQUID [NATURAL CREATIONS, INC.] 5 Current NDC, Legacy NDC, 1 package rows 20241224_37ea5d4c-b443-4465-b97f-449c76f13af9.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 43406-0587-1 43406058701 30 mL in 1 BOTTLE, DROPPER (43406-0587-1) 30 ml 2007-05-29 0000-00-00 No No Current