Home NDC 63083-2144-2 Hyperhidrosis Drops
Product NDC 63083-2144
Requested package NDC 63083-2144-2
11-digit product format 630832144
Labeler code 63083
Product ID 63083-2144_6b2051df-a51c-4046-8def-2573d02f5944
Type HUMAN OTC DRUG
Nonproprietary name Hyperhidrosis Drops
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance ACETIC ACID; LIQUID PETROLEUM; SAMBUCUS NIGRA FLOWERING TOP; GRAPHITE; PHOSPHORIC ACID; SEPIA OFFICINALIS JUICE; VERATRUM ALBUM ROOT; OYSTER SHELL CALCIUM CARBONATE, CRUDE; ACTIVATED CHARCOAL; MERCURIUS SOLUBILIS
Active strength 6; 6; 6; 12; 12; 12; 12; 30; 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
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 Hyperhidrosis Drops
Brand name suffix 2144
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACETIC ACID 6 [hp_X]/59mL LIQUID PETROLEUM 6 [hp_X]/59mL SAMBUCUS NIGRA FLOWERING TOP 6 [hp_X]/59mL GRAPHITE 12 [hp_X]/59mL PHOSPHORIC ACID 12 [hp_X]/59mL SEPIA OFFICINALIS JUICE 12 [hp_X]/59mL VERATRUM ALBUM ROOT 12 [hp_X]/59mL OYSTER SHELL CALCIUM CARBONATE, CRUDE 30 [hp_X]/59mL ACTIVATED CHARCOAL 30 [hp_X]/59mL MERCURIUS SOLUBILIS 30 [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 C144 2026-01-09 C144 2024-01-30 C144 2024-01-30 C144
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-2144-2 Hyperhidrosis Drops2144 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 63083-2144 HYPERHIDROSIS DROPS 2144 (HYPERHIDROSIS DROPS) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220215_bca49d5e-6ade-41d5-82f5-1551936d0a3b.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 63083-2144-2 63083214402 59 mL in 1 BOTTLE, DROPPER (63083-2144-2) 59 ml 1985-08-15 0000-00-00 No No Current