Dr. Talbots Cough Relief

Product NDC
70797-314
11-digit product format
707970314
Labeler code
70797
Product ID
70797-314_cda0f4dc-f551-a6b7-e053-2a95a90a7745
Type
HUMAN OTC DRUG
Nonproprietary name
Antimonium tartaricum, Drosera rotundifolia, Ipecacuanha, Phosphorus, Rumex crispus, Spongia Tosta, Sticta pulmonaria, Kali sulphuricum
Dosage form
LIQUID
Route
ORAL
Labeler
Talbot's Pharmaceuticals Family Products, LLC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2020-07-20
Substance
ANTIMONY TARTRATE ION; DROSERA ROTUNDIFOLIA FLOWERING TOP; IPECAC; PHOSPHORUS; POTASSIUM SULFATE; PULMONARIA OFFICINALIS WHOLE; RUMEX CRISPUS ROOT; SPONGIA OFFICINALIS SKELETON, ROASTED
Active strength
12; 12; 12; 12; 6; 12; 12; 12 [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL
Pharmacologic classes
Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Dr. Talbots Cough Relief
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
PULMONARIA OFFICINALIS WHOLE12 [hp_X]/118mL
ANTIMONY TARTRATE ION12 [hp_X]/118mL
DROSERA ROTUNDIFOLIA FLOWERING TOP12 [hp_X]/118mL
PHOSPHORUS12 [hp_X]/118mL
RUMEX CRISPUS ROOT6 [hp_X]/118mL
POTASSIUM SULFATE12 [hp_X]/118mL
SPONGIA OFFICINALIS SKELETON, ROASTED12 [hp_X]/118mL
IPECAC12 [hp_X]/118mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 8 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
483B0A2Y00Internal UNII lookup
CQN5KB2U1MInternal UNII lookup
75O014T1HGInternal UNII lookup
27YLU75U4WInternal UNII lookup
9N1RM2S62CInternal UNII lookup
1K573LC5TVInternal UNII lookup
1PIP394IIDInternal UNII lookup
62I3C8233LInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
91d3e4d6-356b-4e7f-e053-2a95a90a5158Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
9e37788c-b1bf-42ae-aac9-b60601606144Product name820260122
95250459-30e4-45c1-b08a-993044f49109Product name220250805
d9771140-739b-484b-ae64-b79528ff1211Product name320250801
efd58dcf-540a-4531-8766-e713129ca6f2Product name120250307
1527ac37-808d-43be-a63e-74e1258dbe46Product name920250219
bed0530e-f939-4541-956b-6928a2f6404fProduct name120241008
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name620240814
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
9fcb7a91-de07-4f00-aabf-e4d6fda403d5Product name820230322
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
0ec3537a-6c9b-432a-896c-b9ea8723049aProduct name920200701
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
7916de40-e296-41f0-b811-6d0df1a33e2cProduct name920180627
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name220171212
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
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810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70797-314-01Dr. Talbots Cough Relief1 in 1 CARTONLIQUID13
70797-314-04Dr. Talbots Cough Relief118 mL in 1 BOTTLELIQUID1183

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70797-314DR. TALBOTS COUGH RELIEF (ANTIMONIUM TARTARICUM, DROSERA ROTUNDIFOLIA, IPECACUANHA, PHOSPHORUS, RUMEX CRISPUS, SPONGIA TOSTA, STICTA PULMONARIA, KALI SULPHURICUM) LIQUID [TALBOT'S PHARMACEUTICALS FAMILY PRODUCTS, LLC.]3Current NDC, Legacy NDC, 2 package rows20211006_91d3e4d6-356b-4e7f-e053-2a95a90a5158.zip

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
Dr. Talbots Cough ReliefANTIMONIUM TARTARICUM, DROSERA ROTUNDIFOLIA, IPECACUANHA, PHOSPHORUS, RUMEX CRISPUS, SPONGIA TOSTA, STICTA PULMONARIA, KALI SULPHURICUMTalbot's Pharmaceuticals Family Products, LLC.91d3e4d6-356b-4e7f-e053-2a95a90a51582021-10-05WarningsExact identifier
ndc (product): 70797-314

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70797-314-01707970314011 BOTTLE in 1 CARTON (70797-314-01) / 118 mL in 1 BOTTLE (70797-314-04) 1 bottle2020-07-200000-00-00NoNoCurrent
70797-314-0470797031404118 mL in 1 BOTTLE118 mlHistorical