FDA.reportPublic FDA data

RET Lung

Product NDC
63083-7003
11-digit product format
630837003
Labeler code
63083
Product ID
63083-7003_df48b777-2175-4e9a-8ced-94ff70edfce3
Type
HUMAN OTC DRUG
Nonproprietary name
RET Lung
Dosage form
LIQUID
Route
ORAL
Labeler
Professional Complementary Health Formulas
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1984-08-15
Substance
ANHYDROUS DIBASIC CALCIUM PHOSPHATE; CASTANEA SATIVA FLOWER; CAUSTICUM; CICHORIUM INTYBUS FLOWER; DELPHINIUM STAPHISAGRIA SEED; GOLD; LACHESIS MUTA VENOM; ORNITHOGALUM UMBELLATUM FLOWERING TOP; POTASSIUM PHOSPHATE, UNSPECIFIED FORM; SODIUM CHLORIDE; STRYCHNOS IGNATII SEED
Active strength
3; 3; 30; 3; 30; 30; 30; 3; 3; 30; 30 [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL
Pharmacologic classes
Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
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
RET Lung 7003RET LUNGProfessional Complementary Health Formulas2ed03832-f226-4b3c-9ee6-5352f8d79fdb2026-01-08WarningsExact identifier
ndc (product): 63083-7003

Additional Listing Data#

Finished product
Yes
Brand name base
RET Lung
Brand name suffix
7003
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
CICHORIUM INTYBUS FLOWER3 [hp_X]/29.5mL
ORNITHOGALUM UMBELLATUM FLOWERING TOP3 [hp_X]/29.5mL
CASTANEA SATIVA FLOWER30 [hp_X]/29.5mL
ANHYDROUS DIBASIC CALCIUM PHOSPHATE3 [hp_X]/29.5mL
POTASSIUM PHOSPHATE, UNSPECIFIED FORM30 [hp_X]/29.5mL
GOLD30 [hp_X]/29.5mL
CAUSTICUM30 [hp_X]/29.5mL
STRYCHNOS IGNATII SEED3 [hp_X]/29.5mL
LACHESIS MUTA VENOM3 [hp_X]/29.5mL
SODIUM CHLORIDE30 [hp_X]/29.5mL
DELPHINIUM STAPHISAGRIA SEED30 [hp_X]/29.5mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 11 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
HW54500A89Internal UNII lookup
CZD6M4PY4BInternal UNII lookup
YHZ719F7M3Internal UNII lookup
L11K75P92JInternal UNII lookup
B7862WZ632Internal UNII lookup
79Y1949PYOInternal UNII lookup
DD5FO1WKFUInternal UNII lookup
1NM3M2487KInternal UNII lookup
VSW71SS07IInternal UNII lookup
451W47IQ8XInternal UNII lookup
00543AP1JVInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
2ed03832-f226-4b3c-9ee6-5352f8d79fdbAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
bed0530e-f939-4541-956b-6928a2f6404fProduct name120241008
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name620240814
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name220171212
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
684ea482-2e8b-14af-5664-b98f1e402036Product name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
b060cc1a-fe47-856b-0b77-4448b5963de8Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63083-7003-12026-01-09C16284748780-11030e365-0103-111a-e063-dadaa90a10e2RET3
63083-7003-12026-01-09C16284748780-11030e365-0103-111a-e063-dadaa90a10e2RET3
63083-7003-12024-01-30C16284748780-11030e365-0103-111a-e063-dadaa90a10e2RET3
63083-7003-12024-01-30C16284748780-11030e365-0103-111a-e063-dadaa90a10e2RET3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63083-7003-1RET Lung700329.5 mL in 1 BOTTLE, DROPPERLIQUID29.52

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63083-7003RET LUNG 7003 (RET LUNG) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]1Current NDC, Legacy NDC, 1 package rows20220209_2ed03832-f226-4b3c-9ee6-5352f8d79fdb.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63083-7003-16308370030129.5 mL in 1 BOTTLE, DROPPER (63083-7003-1) 29.5 ml1985-08-150000-00-00NoNoCurrent