FDA.reportPublic FDA data

Lungs and Bronchial Relief

Product NDC
57955-9991
11-digit product format
579559991
Labeler code
57955
Product ID
57955-9991_e3a1f7b0-12dd-49c1-9d0c-6b74fe7ead4e
Type
HUMAN OTC DRUG
Nonproprietary name
Ammonium carbonicum, Antimonium arsenicicum, Antimonium tartaricum, Arsenicum album, Bromium, Carbo vegetabilis, Chlorinum, Kali carbonicum, Lobelia inflata, Stannum metallicum, Sulphuricum acidum.
Dosage form
LIQUID
Route
ORAL
Labeler
King Bio Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2025-10-20
Substance
ACTIVATED CHARCOAL; AMMONIUM CARBONATE; ANTIMONY ARSENATE; ANTIMONY POTASSIUM TARTRATE; ARSENIC TRIOXIDE; BROMINE; CHLORINE; LOBELIA INFLATA WHOLE; POTASSIUM CARBONATE; SULFURIC ACID; TIN
Active strength
10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10 [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
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Lungs and Bronchial Relief
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AMMONIUM CARBONATE10 [hp_X]/59mL
ANTIMONY ARSENATE10 [hp_X]/59mL
ANTIMONY POTASSIUM TARTRATE10 [hp_X]/59mL
ARSENIC TRIOXIDE10 [hp_X]/59mL
BROMINE10 [hp_X]/59mL
ACTIVATED CHARCOAL10 [hp_X]/59mL
CHLORINE10 [hp_X]/59mL
POTASSIUM CARBONATE10 [hp_X]/59mL
LOBELIA INFLATA WHOLE10 [hp_X]/59mL
TIN10 [hp_X]/59mL
SULFURIC ACID10 [hp_X]/59mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 11 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
NJ5VT0FKLJInternal UNII lookup
WE3458XNFTInternal UNII lookup
DL6OZ476V3Internal UNII lookup
S7V92P67HOInternal UNII lookup
SBV4XY874GInternal UNII lookup
2P3VWU3H10Internal UNII lookup
4R7X1O2820Internal UNII lookup
BQN1B9B9HAInternal UNII lookup
9PP1T3TC5UInternal UNII lookup
387GMG9FH5Internal UNII lookup
O40UQP6WCFInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
fc4d4a56-3483-4cae-9818-fdae4e95ec6cAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
57955-9991-2Lungs and Bronchial Relief59 mL in 1 BOTTLE, SPRAYLIQUID592

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.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Lungs and Bronchial ReliefAMMONIUM CARBONICUM, ANTIMONIUM ARSENICICUM, ANTIMONIUM TARTARICUM, ARSENICUM ALBUM, BROMIUM, CARBO VEGETABILIS, CHLORINUM, KALI CARBONICUM, LOBELIA INFLATA, STANNUM METALLICUM, SULPHURICUM ACIDUM.King Bio Inc.fc4d4a56-3483-4cae-9818-fdae4e95ec6c2026-03-02WarningsExact identifier
ndc (product): 57955-9991

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
57955-9991-25795599910259 mL in 1 BOTTLE, SPRAY (57955-9991-2) 59 ml2025-10-20NoNoCurrent