PMS Drops

Product NDC
63083-2124
Requested package NDC
63083-2124-2
11-digit product format
630832124
Labeler code
63083
Product ID
63083-2124_28db45aa-e10e-423d-8c50-0eca2bfeb3ff
Type
HUMAN OTC DRUG
Nonproprietary name
PMS Drops
Dosage form
LIQUID
Route
ORAL
Labeler
Professional Complementary Health Formulas
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1984-08-15
Substance
CHASTE TREE FRUIT; CAULOPHYLLUM THALICTROIDES ROOT; BLACK COHOSH; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; BOS TAURUS PITUITARY GLAND, POSTERIOR; PULSATILLA MONTANA WHOLE; SEPIA OFFICINALIS JUICE; SPONGIA OFFICINALIS SKELETON, ROASTED; THYROID, UNSPECIFIED; VIBURNUM OPULUS BARK; LACHESIS MUTA VENOM; ESTROGENS, CONJUGATED; PROGESTERONE
Active strength
3; 6; 6; 6; 6; 6; 6; 6; 6; 6; 15; 30; 30 [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; [hp_X]/59mL; [hp_X]/59mL
Pharmacologic classes
Calculi Dissolution Agent [EPC], Estrogen Receptor Agonists [MoA], Estrogen [EPC], Estrogens, Conjugated (USP) [CS], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Progesterone [CS], Progesterone [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 15 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Snapshot, Source SHA-256 table
Captured / source dateSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-312ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-100efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-08ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09557ba5c1ecfa…9c80585c8c6e…
2024-05-28 21:12 UTC · source 2024-05-288af77b9d5b6f…d9bbb34c5368…
2024-05-15 03:39 UTC · source 2024-05-14834df4deac94…adcc014656a3…
2024-03-11 06:39 UTC · source 2024-03-081332a3947898…d4bfe170f9cd…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product
Yes
Brand name base
PMS Drops
Brand name suffix
2124
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
CHASTE TREE FRUIT3 [hp_X]/59mL
CAULOPHYLLUM THALICTROIDES ROOT6 [hp_X]/59mL
BLACK COHOSH6 [hp_X]/59mL
MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE6 [hp_X]/59mL
BOS TAURUS PITUITARY GLAND, POSTERIOR6 [hp_X]/59mL
PULSATILLA MONTANA WHOLE6 [hp_X]/59mL
SEPIA OFFICINALIS JUICE6 [hp_X]/59mL
SPONGIA OFFICINALIS SKELETON, ROASTED6 [hp_X]/59mL
THYROID, UNSPECIFIED6 [hp_X]/59mL
VIBURNUM OPULUS BARK6 [hp_X]/59mL
LACHESIS MUTA VENOM15 [hp_X]/59mL
ESTROGENS, CONJUGATED30 [hp_X]/59mL
PROGESTERONE30 [hp_X]/59mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 13 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
433OSF3U8AInternal UNII lookup
JTJ6HH6YEHInternal UNII lookup
K73E24S6X9Internal UNII lookup
HF539G9L3QInternal UNII lookup
7JM57I419KInternal UNII lookup
24K790T39BInternal UNII lookup
QDL83WN8C2Internal UNII lookup
1PIP394IIDInternal UNII lookup
0B4FDL9I6PInternal UNII lookup
T1UG6H6805Internal UNII lookup
VSW71SS07IInternal UNII lookup
IU5QR144QXInternal UNII lookup
4G7DS2Q64YInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
d05bfbbe-d19d-4fd5-8679-bf17d0b61840Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6e3c022f-0786-43f1-8857-edff89d5153fProduct name120260309
95250459-30e4-45c1-b08a-993044f49109Product name220250805
efd58652-cb8f-4018-91ca-4b0eb2ff729fProduct name720240226
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
b46148e2-ee15-98d5-12f0-f5ec8745f6fcProduct name320220927
76820076-f087-4073-b1d1-aa04b361335eProduct name220220921
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
2641ccb3-721d-4fbf-9f2f-ca2f18157a62Product name320210309
d3229c1a-4e51-4e04-9b13-00d24fd35242Product name120200821
213f0591-95c1-b398-40b7-08b31f66b026Product name420190206
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323
d95be220-b30e-4165-a12d-f83825b0efb1Product name120160111
882e78d5-69f7-4a43-812f-1c1628241bbcProduct name120150910
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
e7e58cd3-cacb-49df-8d34-1ee335614abbProduct name120150609
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
2e1ce74f-4938-37b4-e2b4-cfd7971b45eaProduct name120140508
85b2d644-53b2-f2dc-4dbc-859116ce56c0Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
d048f0e3-3c40-8816-8c5c-0ca5cd189aacProduct name120140508
d90784c3-64a2-2f23-9acd-d948d25bf235Product name120140508

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
EffectiveRelated label
2026-01-08C124
2026-01-08C124
2024-01-30C124
2024-01-30C124

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63083-2124-2PMS Drops212459 mL in 1 BOTTLE, DROPPERLIQUID592

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63083-2124PMS DROPS 2124 (PMS DROPS) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]1Current NDC, Legacy NDC, 1 package rows20220216_d05bfbbe-d19d-4fd5-8679-bf17d0b61840.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
PMS Drops 2124PMS DROPSProfessional Complementary Health Formulasd05bfbbe-d19d-4fd5-8679-bf17d0b618402026-01-08WarningsExact identifier
ndc (package): 63083-2124-2
ndc (product): 63083-2124
ndc11 (package): 63083212402

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63083-2124-26308321240259 mL in 1 BOTTLE, DROPPER (63083-2124-2) 59 ml1985-08-150000-00-00NoNoCurrent