Home NDC 63083-2175-2 Rehydration Drops
Product NDC 63083-2175
Requested package NDC 63083-2175-2
11-digit product format 630832175
Labeler code 63083
Product ID 63083-2175_c17c623a-dc46-479f-b32c-e716422e4dbf
Type HUMAN OTC DRUG
Nonproprietary name Rehydration Drops
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance .GAMMA.-AMINOBUTYRIC ACID; ADENOSINE TRIPHOSPHATE; ARABICA COFFEE BEAN; BEEF KIDNEY; BOS TAURUS HYPOTHALAMUS; GERMANIUM; HYPERICUM PERFORATUM WHOLE; SEROTONIN; SILICON DIOXIDE; SUS SCROFA ADRENAL GLAND; TARAXACUM OFFICINALE
Active strength 6; 4; 1; 6; 6; 12; 3; 12; 4; 6; 1 [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 Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], 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 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…
Additional Listing Data#
Finished product Yes
Brand name base Rehydration Drops
Brand name suffix 2175
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ARABICA COFFEE BEAN 6 [hp_X]/59mL TARAXACUM OFFICINALE 4 [hp_X]/59mL HYPERICUM PERFORATUM WHOLE 1 [hp_X]/59mL ADENOSINE TRIPHOSPHATE 6 [hp_X]/59mL SILICON DIOXIDE 6 [hp_X]/59mL SUS SCROFA ADRENAL GLAND 12 [hp_X]/59mL BOS TAURUS HYPOTHALAMUS 3 [hp_X]/59mL BEEF KIDNEY 12 [hp_X]/59mL .GAMMA.-AMINOBUTYRIC ACID 4 [hp_X]/59mL GERMANIUM 6 [hp_X]/59mL SEROTONIN 1 [hp_X]/59mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 11 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 C175 2026-01-09 C175 2024-01-30 C175 2024-01-30 C175
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-2175-2 Rehydration Drops2175 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 63083-2175 REHYDRATION DROPS 2175 (REHYDRATION DROPS) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220216_58cc2bd1-c530-43bf-876e-f30d4d95b8da.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 63083-2175-2 63083217502 59 mL in 1 BOTTLE, DROPPER (63083-2175-2) 59 ml 1985-08-15 0000-00-00 No No Current