Hyperthyroid Drops

Product NDC: 63083-2029
11-digit product format: 630832029
Labeler code: 63083
Product ID: 63083-2029_289f2400-c0ff-4e74-9fc4-e7979e0b8970
Type: HUMAN OTC DRUG
Nonproprietary name: Hyperthyroid Drops
Dosage form: LIQUID
Route: ORAL
Labeler: Professional Complementary Health Formulas
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start: 1984-08-15
Substance: ACTIVATED CHARCOAL; APIS MELLIFERA; BOS TAURUS PITUITARY GLAND, POSTERIOR; CONIUM MACULATUM FLOWERING TOP; LACHESIS MUTA VENOM; LYCOPUS VIRGINICUS WHOLE; PHOSPHORUS; POTASSIUM IODIDE; SPONGIA OFFICINALIS SKELETON, ROASTED
Active strength: 3; 3; 6; 6; 8; 2; 6; 2; 4 [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], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Standardized Insect Venom 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 · 30 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	63083-2029-2	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	63083-2029-2	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	63083-2029-2	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	63083-2029-2	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	63083-2029-2	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	63083-2029-2	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	63083-2029-2	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	63083-2029-2	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	63083-2029-2	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded product	product		`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	63083-2029-2	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded product	product		`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	63083-2029-2	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded product	product		`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	63083-2029-2	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded product	product		`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded package	package	63083-2029-2	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded product	product		`834df4deac94…`	`adcc014656a3…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded package	package	63083-2029-2	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded product	product		`1332a3947898…`	`d4bfe170f9cd…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded package	package	63083-2029-2	`1332a3947898…`	`d4bfe170f9cd…`

Additional Listing Data#

Finished product: Yes
Brand name base: Hyperthyroid Drops
Brand name suffix: 2029
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
POTASSIUM IODIDE	3 [hp_X]/59mL
LYCOPUS VIRGINICUS WHOLE	3 [hp_X]/59mL
APIS MELLIFERA	6 [hp_X]/59mL
ACTIVATED CHARCOAL	6 [hp_X]/59mL
SPONGIA OFFICINALIS SKELETON, ROASTED	8 [hp_X]/59mL
CONIUM MACULATUM FLOWERING TOP	2 [hp_X]/59mL
PHOSPHORUS	6 [hp_X]/59mL
BOS TAURUS PITUITARY GLAND, POSTERIOR	2 [hp_X]/59mL
LACHESIS MUTA VENOM	4 [hp_X]/59mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 9 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1C4QK22F9J	Internal UNII lookup
TWH5125Q6F	Internal UNII lookup
7S82P3R43Z	Internal UNII lookup
2P3VWU3H10	Internal UNII lookup
1PIP394IID	Internal UNII lookup
Q28R5GF371	Internal UNII lookup
27YLU75U4W	Internal UNII lookup
7JM57I419K	Internal UNII lookup
VSW71SS07I	Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
be6f64dd-946b-4933-abb7-7b4c095c2490	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
Effective	Related label
2026-01-08	C29
2026-01-08	C29
2024-01-30	C29
2024-01-30	C29

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
63083-2029-2	Hyperthyroid Drops2029	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
63083-2029	HYPERTHYROID DROPS 2029 (HYPERTHYROID DROPS) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]	1	Current NDC, Legacy NDC, 1 package rows	20220215_be6f64dd-946b-4933-abb7-7b4c095c2490.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.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Hyperthyroid Drops 2029	HYPERTHYROID DROPS	Professional Complementary Health Formulas	be6f64dd-946b-4933-abb7-7b4c095c2490	2026-01-08	Warnings	Exact identifier ndc (product): 63083-2029

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
2P3VWU3H10	ACTIVATED CHARCOAL	64365-11-3	ACTIVATED CHARCOAL
7S82P3R43Z	APIS MELLIFERA		APIS MELLIFERA
7JM57I419K	BOS TAURUS PITUITARY GLAND, POSTERIOR		BOS TAURUS PITUITARY GLAND, POSTERIOR
Q28R5GF371	CONIUM MACULATUM FLOWERING TOP		CONIUM MACULATUM FLOWERING TOP
VSW71SS07I	LACHESIS MUTA VENOM		LACHESIS MUTA VENOM
27YLU75U4W	PHOSPHORUS	7723-14-0	PHOSPHORUS
1C4QK22F9J	POTASSIUM IODIDE	7681-11-0	POTASSIUM IODIDE
1PIP394IID	SPONGIA OFFICINALIS SKELETON, ROASTED		SPONGIA OFFICINALIS SKELETON, ROASTED

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
63083-2029-2	63083202902	59 mL in 1 BOTTLE, DROPPER (63083-2029-2)	59 ml	1985-08-15	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
C29	Professional Complementary Health Formulas \| Natural Pharmaceutical Manufacturing LLC	2026-01-08	HUMAN OTC DRUG LABEL	2