Home NDC 63083-2001-2 Acne Drops
Product NDC 63083-2001
Requested package NDC 63083-2001-2
11-digit product format 630832001
Labeler code 63083
Product ID 63083-2001_1876968d-0cad-46ed-9cb5-b5ab85ffa3d8
Type HUMAN OTC DRUG
Nonproprietary name Acne Drops
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance ANTIMONY TRISULFIDE; ARCTIUM LAPPA ROOT OIL; BERBERIS AQUIFOLIUM ROOT BARK; CARBO ANIMALIS; CENTELLA ASIATICA LEAF; POTASSIUM BROMIDE; RHODODENDRON TOMENTOSUM LEAFY TWIG; SANGUINARIA CANADENSIS ROOT; SILICON DIOXIDE; SODIUM CHLORIDE; STRYCHNOS NUX-VOMICA SEED; SULFUR
Active strength 8; 3; 3; 15; 3; 12; 4; 6; 6; 12; 6; 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; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], 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 Acne Drops
Brand name suffix 2001
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ARCTIUM LAPPA ROOT OIL 8 [hp_X]/59mL BERBERIS AQUIFOLIUM ROOT BARK 3 [hp_X]/59mL CENTELLA ASIATICA LEAF 3 [hp_X]/59mL RHODODENDRON TOMENTOSUM LEAFY TWIG 15 [hp_X]/59mL STRYCHNOS NUX-VOMICA SEED 3 [hp_X]/59mL SANGUINARIA CANADENSIS ROOT 12 [hp_X]/59mL SILICON DIOXIDE 4 [hp_X]/59mL SULFUR 6 [hp_X]/59mL ANTIMONY TRISULFIDE 6 [hp_X]/59mL POTASSIUM BROMIDE 12 [hp_X]/59mL SODIUM CHLORIDE 6 [hp_X]/59mL CARBO ANIMALIS 6 [hp_X]/59mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 12 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 2026-01-08 C1 2026-01-08 C1 2024-01-30 C1 2024-01-30 C1
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-2001-2 Acne Drops2001 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 63083-2001 ACNE DROPS 2001 (ACNE DROPS) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220215_340fc7dc-2aa4-411f-842b-4ce704671722.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 63083-2001-2 63083200102 59 mL in 1 BOTTLE, DROPPER (63083-2001-2) 59 ml 1985-08-15 0000-00-00 No No Current