ALLERGY ATLANTIC MOLD MIX

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: ALLERGY ATLANTIC MOLD MIX
Generic name: ALTERNARIA ALTERNATA, ASPERGILLUS FUMIGATUS, BOTRYTIS CINEREA, RHIZOPUS STOLONIFER, USTILAGO MAYDIS
Manufacturer: Natural Creations, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 37ea5d4c-b443-4465-b97f-449c76f13af9
SPL ID: e1267a37-7517-45f6-aaf8-0b490255e8a4
Version: 5
Effective date: 2024-12-19
Source export date: 2026-10-12
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:53:00

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 13 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		ALLERGY ATLANTIC MOLD MIX	openfda.brand_name
generic name		ALTERNARIA ALTERNATA, ASPERGILLUS FUMIGATUS, BOTRYTIS CINEREA, RHIZOPUS STOLONIFER, USTILAGO MAYDIS	openfda.generic_name
manufacturer name		Natural Creations, Inc.	openfda.manufacturer_name
ndc	package	43406-0587-1	openfda.package_ndc
ndc	product	43406-0587	openfda.product_ndc
ndc11	package	43406058701	derived:openfda.package_ndc
spl id		e1267a37-7517-45f6-aaf8-0b490255e8a4	id
spl set id		37ea5d4c-b443-4465-b97f-449c76f13af9	set_id
unii		4K7Z7K7SWG	openfda.unii
unii		TBW53313S7	openfda.unii
unii		FEE198DK4Q	openfda.unii
unii		52B29REC7H	openfda.unii
unii		X88DF51T48	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS: *Consult a physician for use in children under 12 years of age. * IF PREGNANT OR BREAST-FEEDING, ask a health care professional before use. * KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away. * Do not use if TAMPER EVIDENT seal is broken or missing.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.