Tinnitus Drops

Product NDC: 63083-2072
11-digit product format: 630832072
Labeler code: 63083
Product ID: 63083-2072_81eecf06-9f70-47e0-9b9c-3dd85170255a
Type: HUMAN OTC DRUG
Nonproprietary name: Tinnitus Drops
Dosage form: LIQUID
Route: ORAL
Labeler: Professional Complementary Health Formulas
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start: 1984-08-15
Substance: BLACK COHOSH; GINKGO; CINCHONA OFFICINALIS BARK; GOLDENSEAL; SUS SCROFA EAR; LYCOPODIUM CLAVATUM SPORE; BOS TAURUS NERVE; SULFUR; DIGITALIS; POTASSIUM CARBONATE
Active strength: 1; 1; 3; 5; 6; 6; 6; 6; 12; 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 · 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	63083-2072-2	`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	63083-2072-2	`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	63083-2072-2	`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	63083-2072-2	`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	63083-2072-2	`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	63083-2072-2	`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	63083-2072-2	`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	63083-2072-2	`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	63083-2072-2	`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	63083-2072-2	`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	63083-2072-2	`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	63083-2072-2	`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	63083-2072-2	`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	63083-2072-2	`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	63083-2072-2	`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: Tinnitus Drops
Brand name suffix: 2072
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
BLACK COHOSH	1 [hp_X]/59mL
GINKGO	1 [hp_X]/59mL
CINCHONA OFFICINALIS BARK	3 [hp_X]/59mL
GOLDENSEAL	5 [hp_X]/59mL
SUS SCROFA EAR	6 [hp_X]/59mL
LYCOPODIUM CLAVATUM SPORE	6 [hp_X]/59mL
BOS TAURUS NERVE	6 [hp_X]/59mL
SULFUR	6 [hp_X]/59mL
DIGITALIS	12 [hp_X]/59mL
POTASSIUM CARBONATE	30 [hp_X]/59mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 10 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
K73E24S6X9	Internal UNII lookup
19FUJ2C58T	Internal UNII lookup
S003A158SB	Internal UNII lookup
ZW3Z11D0JV	Internal UNII lookup
7DX2J287CV	Internal UNII lookup
C88X29Y479	Internal UNII lookup
28G2U3MQJK	Internal UNII lookup
70FD1KFU70	Internal UNII lookup
F1T8QT9U8B	Internal UNII lookup
BQN1B9B9HA	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
24649b5b-ed21-4a32-8501-196b9e1348bb	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
Effective	Related label
2026-01-09	C72
2026-01-09	C72
2024-01-30	C72
2024-01-30	C72

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
63083-2072-2	Tinnitus Drops2072	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
63083-2072	TINNITUS DROPS 2072 (TINNITUS DROPS) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]	1	Current NDC, Legacy NDC, 1 package rows	20220216_24649b5b-ed21-4a32-8501-196b9e1348bb.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
Tinnitus Drops 2072	TINNITUS DROPS	Professional Complementary Health Formulas	24649b5b-ed21-4a32-8501-196b9e1348bb	2026-01-08	Warnings	Exact identifier ndc (product): 63083-2072

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
K73E24S6X9	BLACK COHOSH		BLACK COHOSH
19FUJ2C58T	GINKGO	90045-36-6	GINKGO
S003A158SB	CINCHONA OFFICINALIS BARK		CINCHONA OFFICINALIS BARK
ZW3Z11D0JV	GOLDENSEAL		GOLDENSEAL
7DX2J287CV	SUS SCROFA EAR		SUS SCROFA EAR
C88X29Y479	LYCOPODIUM CLAVATUM SPORE	8023-70-9	LYCOPODIUM CLAVATUM SPORE
28G2U3MQJK	BOS TAURUS NERVE		BOS TAURUS NERVE
70FD1KFU70	SULFUR	7704-34-9	SULFUR
F1T8QT9U8B	DIGITALIS	8031-42-3	DIGITALIS
BQN1B9B9HA	POTASSIUM CARBONATE	584-08-7	POTASSIUM CARBONATE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
63083-2072-2	63083207202	59 mL in 1 BOTTLE, DROPPER (63083-2072-2)	59 ml	1985-08-15	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
C72	Professional Complementary Health Formulas \| Natural Pharmaceutical Manufacturing LLC	2026-01-08	HUMAN OTC DRUG LABEL	2