Pneumotox

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: Pneumotox
Generic name: TRITICUM AESTIVUM, ALFALFA, ARNICA MONTANA, ASCLEPIAS TUBEROSA, CHAMOMILLA, ECHINACEA (ANGUSTIFOLIA), EUCALYPTUS GLOBULUS, FUCUS VESICULOSUS, HORDEUM VULGARE, IODIUM, NASTURTIUM AQUATICUM, PLANTAGO MAJOR, RAPHANUS SATIVUS, TRIFOLIUM PRATENSE, TRIGONELLA FOENUM-GRAECUM, SYMPHYTUM OFFICINALE, LUNG (SUIS), ORYZA SATIVA, SILICEA, ACETONE, SODIUM TRIPOLYPHOSPHATE, PROPYLENE GLYCOL, BENZINUM, AMMONIUM MURIATICUM, SODIUM LAURYL SULFATE, TEREBINTHINA, ARSENICUM ALBUM, NATRUM MURIATICUM, NITRICUM ACIDUM,
Manufacturer: BioActive Nutritional, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: f8846fb1-92e5-4f8e-b3b3-bc620df90a62
SPL ID: 4c238e58-9f3d-4061-beb8-fd1a7107061e
Version: 4
Effective date: 2023-07-12
Source export date: 2026-11-06
Source partition: 10
Source file: https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/3b52cde3709f43d454872fcaffdb78395b270bc65272c06ef1005cc77c998864/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: 8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
Import run: 20261106T075659Z
Imported at: 2026-11-06 09:00:08

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 2 · 42 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Pneumotox	openfda.brand_name
generic name		TRITICUM AESTIVUM, ALFALFA, ARNICA MONTANA, ASCLEPIAS TUBEROSA, CHAMOMILLA, ECHINACEA (ANGUSTIFOLIA), EUCALYPTUS GLOBULUS, FUCUS VESICULOSUS, HORDEUM VULGARE, IODIUM, NASTURTIUM AQUATICUM, PLANTAGO MAJOR, RAPHANUS SATIVUS, TRIFOLIUM PRATENSE, TRIGONELLA FOENUM-GRAECUM, SYMPHYTUM OFFICINALE, LUNG (SUIS), ORYZA SATIVA, SILICEA, ACETONE, SODIUM TRIPOLYPHOSPHATE, PROPYLENE GLYCOL, BENZINUM, AMMONIUM MURIATICUM, SODIUM LAURYL SULFATE, TEREBINTHINA, ARSENICUM ALBUM, NATRUM MURIATICUM, NITRICUM ACIDUM,	openfda.generic_name
manufacturer name		BioActive Nutritional, Inc.	openfda.manufacturer_name
ndc	package	43857-0533-1	openfda.package_ndc
ndc	product	43857-0533	openfda.product_ndc
ndc11	package	43857053301	derived:openfda.package_ndc
spl id		4c238e58-9f3d-4061-beb8-fd1a7107061e	id
spl set id		f8846fb1-92e5-4f8e-b3b3-bc620df90a62	set_id
unii		27YLU75U4W	openfda.unii
unii		01Q9PC255D	openfda.unii
unii		1ZL82U5D18	openfda.unii
unii		7GL3G1COB3	openfda.unii
unii		6DC9Q167V3	openfda.unii
unii		86R5J6D01D	openfda.unii
unii		3C3Y389JBU	openfda.unii
unii		DJO934BRBD	openfda.unii
unii		O80TY208ZW	openfda.unii
unii		411VRN1TV4	openfda.unii
unii		5HK03SA80J	openfda.unii
unii		9679TC07X4	openfda.unii
unii		ETJ7Z6XBU4	openfda.unii
unii		451W47IQ8X	openfda.unii
unii		W2469WNO6U	openfda.unii
unii		6IO182RP7A	openfda.unii
unii		S7V92P67HO	openfda.unii
unii		VB06AV5US8	openfda.unii
unii		J64922108F	openfda.unii
unii		1364PS73AF	openfda.unii
unii		N4LEE4Z93J	openfda.unii
unii		535G2ABX9M	openfda.unii
unii		8E272251DI	openfda.unii
unii		368GB5141J	openfda.unii
unii		84IVV0906Z	openfda.unii
unii		E4GA8884NN	openfda.unii
unii		YH89GMV676	openfda.unii
unii		86507VZR9K	openfda.unii
unii		4JS0838828	openfda.unii
unii		G0R4UBI2ZZ	openfda.unii
unii		5610HF69OB	openfda.unii
unii		S546YLW6E6	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: If pregnant or breast-feeding, ask a health care professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Do not use if tamper evident seal is broken or missing. Store in cool, dry place.

Reported adverse events (FAERS/openFDA)#

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