FDA.reportPublic FDA data

Abdominal Pain Drops

Product NDC
63083-2051
11-digit product format
630832051
Labeler code
63083
Product ID
63083-2051_d726dade-f77f-4db7-a445-08ae30d01b06
Type
HUMAN OTC DRUG
Nonproprietary name
Abdominal Pain Drops
Dosage form
LIQUID
Route
ORAL
Labeler
Professional Complementary Health Formulas
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1984-08-15
Substance
ACTIVATED CHARCOAL; ARTEMISIA ANNUA FLOWERING TOP; BOS TAURUS SOLAR PLEXUS; HYDROCHLORIC ACID; LYCOPODIUM CLAVATUM SPORE; SODIUM SULFATE; STRYCHNOS NUX-VOMICA SEED; SUS SCROFA PARASYMPATHETIC NERVE; TRIPE
Active strength
6; 3; 6; 12; 5; 6; 30; 6; 6 [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
Pharmacologic classes
Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Abdominal Pain Drops
Brand name suffix
2051
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ACTIVATED CHARCOAL6 [hp_X]/59mL
ARTEMISIA ANNUA FLOWERING TOP3 [hp_X]/59mL
BOS TAURUS SOLAR PLEXUS6 [hp_X]/59mL
HYDROCHLORIC ACID12 [hp_X]/59mL
LYCOPODIUM CLAVATUM SPORE5 [hp_X]/59mL
SODIUM SULFATE6 [hp_X]/59mL
STRYCHNOS NUX-VOMICA SEED30 [hp_X]/59mL
SUS SCROFA PARASYMPATHETIC NERVE6 [hp_X]/59mL
TRIPE6 [hp_X]/59mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii2P3VWU3H10, 0UQK6O82OW, Y8H8S1X8IB, QTT17582CB, C88X29Y479, 0YPR65R21J, 269XH13919, 5AZZ2GHR69, C46FS57S0X

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
95250459-30e4-45c1-b08a-993044f49109Product name220250805
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63083-2051-22026-01-09C16284748780-11030e364-fd22-111a-e063-dadaa90a10e2C51
63083-2051-22026-01-09C16284748780-11030e364-fd22-111a-e063-dadaa90a10e2C51
63083-2051-22024-01-30C16284748780-11030e364-fd22-111a-e063-dadaa90a10e2C51
63083-2051-22024-01-30C16284748780-11030e364-fd22-111a-e063-dadaa90a10e2C51

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63083-2051-2Abdominal Pain Drops205159 mL in 1 BOTTLE, DROPPERLIQUID592

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63083-2051ABDOMINAL PAIN DROPS 2051 (ABDOMINAL PAIN DROPS) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]1Current NDC, Legacy NDC, 1 package rows20220215_f1b1dde6-bb37-4774-a58c-b4f648f9c2b5.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63083-2051-26308320510259 mL in 1 BOTTLE, DROPPER (63083-2051-2) 59 ml1985-08-150000-00-00NoNoCurrent