FDA.reportPublic FDA data

Heart/Lung Drops

Product NDC
63083-5007
11-digit product format
630835007
Labeler code
63083
Product ID
63083-5007_bc129b02-c437-4eac-929f-f3c1a7452b19
Type
HUMAN OTC DRUG
Nonproprietary name
Heart/Lung Drops
Dosage form
LIQUID
Route
ORAL
Labeler
Professional Complementary Health Formulas
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1984-08-15
Substance
BEEF HEART; BEEF LUNG; DIGITALIS; FERROSOFERRIC PHOSPHATE; LACHESIS MUTA VENOM
Active strength
6; 6; 12; 6; 12 [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

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Heart/Lung Drops 5007HEART/LUNG DROPSProfessional Complementary Health Formulas365ea750-f5a7-4e50-8ae7-80509e45d5802026-01-08WarningsExact identifier
ndc (product): 63083-5007

Additional Listing Data#

Finished product
Yes
Brand name base
Heart/Lung Drops
Brand name suffix
5007
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
FERROSOFERRIC PHOSPHATE6 [hp_X]/59mL
BEEF HEART6 [hp_X]/59mL
BEEF LUNG12 [hp_X]/59mL
DIGITALIS6 [hp_X]/59mL
LACHESIS MUTA VENOM12 [hp_X]/59mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 5 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
91GQH8I5F7Internal UNII lookup
P47W069U38Internal UNII lookup
2I1RTO1MBRInternal UNII lookup
F1T8QT9U8BInternal UNII lookup
VSW71SS07IInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
365ea750-f5a7-4e50-8ae7-80509e45d580Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63083-5007-22026-01-09C16284748780-11030e365-6de8-111a-e063-dadaa90a10e2HHL
63083-5007-22026-01-09C16284748780-11030e365-6de8-111a-e063-dadaa90a10e2HHL
63083-5007-22024-01-30C16284748780-11030e365-6de8-111a-e063-dadaa90a10e2HHL
63083-5007-22024-01-30C16284748780-11030e365-6de8-111a-e063-dadaa90a10e2HHL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63083-5007-2Heart/Lung Drops500759 mL in 1 BOTTLE, DROPPERLIQUID592

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63083-5007HEART/LUNG DROPS 5007 (HEART/LUNG DROPS) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]1Current NDC, Legacy NDC, 1 package rows20220211_365ea750-f5a7-4e50-8ae7-80509e45d580.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63083-5007-26308350070259 mL in 1 BOTTLE, DROPPER (63083-5007-2) 59 ml1985-08-150000-00-00NoNoCurrent