Home NDC 63083-2105-2 Uterine Formula
Product NDC 63083-2105
Requested package NDC 63083-2105-2
11-digit product format 630832105
Labeler code 63083
Product ID 63083-2105_b6ffdc9f-9570-4b8b-bb3d-a77236ac48d4
Type HUMAN OTC DRUG
Nonproprietary name Uterine Formula
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance LINDERA AGGREGATA ROOT; VITEX NEGUNDO FRUIT; ACONITUM CARMICHAELI LATERAL ROOT; CINNAMOMUM CASSIA TWIG; CROCUS SATIVUS FLOWER; PHELLODENDRON CHINENSIS BARK; CRASSOSTREA GIGAS SHELL; VISCUM ALBUM FRUITING TOP; ASTRAGALUS PROPINQUUS ROOT
Active strength 1; 1; 3; 3; 3; 3; 3; 3; 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
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 date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 1332a3947898…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 Uterine Formula
Brand name suffix 2105
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LINDERA AGGREGATA ROOT 1 [hp_X]/59mL VITEX NEGUNDO FRUIT 1 [hp_X]/59mL ACONITUM CARMICHAELI LATERAL ROOT 3 [hp_X]/59mL CINNAMOMUM CASSIA TWIG 3 [hp_X]/59mL CROCUS SATIVUS FLOWER 3 [hp_X]/59mL PHELLODENDRON CHINENSIS BARK 3 [hp_X]/59mL CRASSOSTREA GIGAS SHELL 3 [hp_X]/59mL VISCUM ALBUM FRUITING TOP 3 [hp_X]/59mL ASTRAGALUS PROPINQUUS ROOT 6 [hp_X]/59mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 9 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# Effective, Related label table Effective Related label 2026-01-09 C105 2026-01-09 C105 2024-01-30 C105 2024-01-30 C105
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-2105-2 Uterine Formula2105 59 mL in 1 BOTTLE, DROPPER LIQUID 59 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63083-2105 UTERINE FORMULA 2105 (UTERINE FORMULA) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220216_0416d627-6ac8-4fcc-8f54-797ddfcaf3e7.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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 63083-2105-2 63083210502 59 mL in 1 BOTTLE, DROPPER (63083-2105-2) 59 ml 1985-08-15 0000-00-00 No No Current