Home NDC 63083-2079-2 Nausea/Morning Sickness Drops
Product NDC 63083-2079
Requested package NDC 63083-2079-2
11-digit product format 630832079
Labeler code 63083
Product ID 63083-2079_a38742d2-8ffe-41c2-86e4-7f62c301ae3f
Type HUMAN OTC DRUG
Nonproprietary name Nausea/Morning Sickness Drops
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance CUCURBITA PEPO SUBSP. OVIFERA WHOLE; SYMPHORICARPOS ALBUS FRUIT; ANAMIRTA COCCULUS FRUIT; IPECAC; PULSATILLA MONTANA WHOLE; PEACH; CEROUS OXALATE NONAHYDRATE; GOSSYPIUM HERBACEUM ROOT BARK; LOBELIA INFLATA WHOLE
Active strength 3; 3; 5; 6; 6; 12; 12; 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
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Fruit Proteins [EXT], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [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 Nausea/Morning Sickness Drops
Brand name suffix 2079
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CUCURBITA PEPO SUBSP. OVIFERA WHOLE 3 [hp_X]/59mL SYMPHORICARPOS ALBUS FRUIT 3 [hp_X]/59mL ANAMIRTA COCCULUS FRUIT 5 [hp_X]/59mL IPECAC 6 [hp_X]/59mL PULSATILLA MONTANA WHOLE 6 [hp_X]/59mL PEACH 12 [hp_X]/59mL CEROUS OXALATE NONAHYDRATE 12 [hp_X]/59mL GOSSYPIUM HERBACEUM ROOT BARK 12 [hp_X]/59mL LOBELIA INFLATA WHOLE 12 [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.
FDA-Initiated Inactive NDC Indexing# Effective, Related label table Effective Related label 2026-01-09 C79 2026-01-09 C79 2024-01-30 C79 2024-01-30 C79
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-2079-2 Nausea/Morning Sickness Drops2079 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 63083-2079 NAUSEA/MORNING SICKNESS DROPS 2079 (NAUSEA/MORNING SICKNESS DROPS) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220216_fd4f2738-9bdc-4fa0-bd61-c69ea4f1cf0f.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 63083-2079-2 63083207902 59 mL in 1 BOTTLE, DROPPER (63083-2079-2) 59 ml 1985-08-15 0000-00-00 No No Current