Home NDC 63083-7305-1 Fifth Chakra (Throat)
Product NDC 63083-7305
Requested package NDC 63083-7305-1
11-digit product format 630837305
Labeler code 63083
Product ID 63083-7305_ea514c0b-528c-4b19-b7b3-3725b429adf0
Type HUMAN OTC DRUG
Nonproprietary name Fifth Chakra (Throat)
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance ANHYDROUS DIBASIC CALCIUM PHOSPHATE; SODIUM SULFATE; SILICON DIOXIDE; SPIGELIA ANTHELMIA WHOLE; COLCHICUM AUTUMNALE BULB; NAJA NAJA VENOM; NERIUM OLEANDER WHOLE; CARBO ANIMALIS; CORALLIUM RUBRUM EXOSKELETON; CALCIUM HEXAFLUOROSILICATE; MALACHITE GREEN; SODIUM
Active strength 8; 8; 8; 8; 12; 12; 12; 15; 15; 30; 30; 30 [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL
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 Fifth Chakra (Throat)
Brand name suffix 7305
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ANHYDROUS DIBASIC CALCIUM PHOSPHATE 8 [hp_X]/29.5mL SODIUM SULFATE 8 [hp_X]/29.5mL SILICON DIOXIDE 8 [hp_X]/29.5mL SPIGELIA ANTHELMIA WHOLE 8 [hp_X]/29.5mL COLCHICUM AUTUMNALE BULB 12 [hp_X]/29.5mL NAJA NAJA VENOM 12 [hp_X]/29.5mL NERIUM OLEANDER WHOLE 12 [hp_X]/29.5mL CARBO ANIMALIS 15 [hp_X]/29.5mL CORALLIUM RUBRUM EXOSKELETON 15 [hp_X]/29.5mL CALCIUM HEXAFLUOROSILICATE 30 [hp_X]/29.5mL MALACHITE GREEN 30 [hp_X]/29.5mL SODIUM 30 [hp_X]/29.5mL
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 2026-01-09 RCT5 2026-01-09 RCT5 2024-01-30 RCT5 2024-01-30 RCT5
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-7305-1 Fifth Chakra (Throat)7305 29.5 mL in 1 BOTTLE, DROPPER LIQUID 29.5 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63083-7305 FIFTH CHAKRA (THROAT) 7305 (FIFTH CHAKRA (THROAT)) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220209_b731f708-10a8-451f-8550-1e7302102b96.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 63083-7305-1 63083730501 29.5 mL in 1 BOTTLE, DROPPER (63083-7305-1) 29.5 ml 1985-08-15 0000-00-00 No No Current