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
IngredientStrength
ALTERNARIA ALTERNATA8 [hp_X]/mL
ASPERGILLUS FUMIGATUS8 [hp_X]/mL
BOTRYTIS CINEREA8 [hp_X]/mL
RHIZOPUS STOLONIFER8 [hp_X]/mL
USTILAGO MAYDIS8 [hp_X]/mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii52B29REC7H, X88DF51T48, TBW53313S7, FEE198DK4Q, 4K7Z7K7SWG

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43406-0587-12022-02-17C16284748780-1d6a99b39-51e3-a426-e053-dadaa90af4c2ALLERGY ATLANTIC MOLD MIX
43406-0587-12022-01-28C16284748780-1d6a99b39-51e3-a426-e053-dadaa90af4c2ALLERGY ATLANTIC MOLD MIX

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43406-0587-1ALLERGY ATLANTIC MOLD MIX30 mL in 1 BOTTLE, DROPPERLIQUID305

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43406-0587ALLERGY ATLANTIC MOLD MIX (ALTERNARIA ALTERNATA, ASPERGILLUS FUMIGATUS, BOTRYTIS CINEREA, RHIZOPUS STOLONIFER, USTILAGO MAYDIS) LIQUID [NATURAL CREATIONS, INC.]5Current NDC, Legacy NDC, 1 package rows20241224_37ea5d4c-b443-4465-b97f-449c76f13af9.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
43406-0587-14340605870130 mL in 1 BOTTLE, DROPPER (43406-0587-1) 30 ml2007-05-290000-00-00NoNoCurrent