Home NDC 63083-2120-2 Teething Drops
Product NDC 63083-2120
Requested package NDC 63083-2120-2
11-digit product format 630832120
Labeler code 63083
Product ID 63083-2120_f97c3e15-b5fe-476d-9cb4-4d565dd902d0
Type HUMAN OTC DRUG
Nonproprietary name Teething Drops
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance EUGENOL; ULMUS RUBRA BARK; ARTEMISIA ANNUA FLOWERING TOP; MENTHA X PIPERITA WHOLE; CLEMATIS RECTA FLOWERING TOP; CITRULLUS COLOCYNTHIS FRUIT PULP; COPPER; MYRRH; BRYONIA ALBA ROOT; OYSTER SHELL CALCIUM CARBONATE, CRUDE
Active strength 3; 3; 3; 4; 6; 6; 6; 6; 12; 12 [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 Allergens [CS], Cell-mediated Immunity [PE], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Increased Histamine Release [PE], Inhibit Ovum Fertilization [PE], Standardized Chemical Allergen [EPC]
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 Teething Drops
Brand name suffix 2120
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength EUGENOL 3 [hp_X]/59mL ULMUS RUBRA BARK 3 [hp_X]/59mL ARTEMISIA ANNUA FLOWERING TOP 3 [hp_X]/59mL MENTHA X PIPERITA WHOLE 4 [hp_X]/59mL CLEMATIS RECTA FLOWERING TOP 6 [hp_X]/59mL CITRULLUS COLOCYNTHIS FRUIT PULP 6 [hp_X]/59mL COPPER 6 [hp_X]/59mL MYRRH 6 [hp_X]/59mL BRYONIA ALBA ROOT 12 [hp_X]/59mL OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X]/59mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 10 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 C120 2026-01-09 C120 2024-01-30 C120 2024-01-30 C120
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-2120-2 Teething Drops2120 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 63083-2120 TEETHING DROPS 2120 (TEETHING DROPS) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220216_31644007-d0a9-4482-a6b4-555b70686a72.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 63083-2120-2 63083212002 59 mL in 1 BOTTLE, DROPPER (63083-2120-2) 59 ml 1985-08-15 0000-00-00 No No Current