Glaucoma Drops

Product NDC: 63083-2074
11-digit product format: 630832074
Labeler code: 63083
Product ID: 63083-2074_617f1878-a655-425b-a81f-a979be629a44
Type: HUMAN OTC DRUG
Nonproprietary name: Glaucoma Drops
Dosage form: LIQUID
Route: ORAL
Labeler: Professional Complementary Health Formulas
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start: 1984-08-15
Substance: PLECTRANTHUS BARBATUS ROOT OIL; BILBERRY; EUPHRASIA STRICTA; GELSEMIUM SEMPERVIRENS ROOT; SPIGELIA ANTHELMIA WHOLE; GOLDENSEAL; ACONITUM NAPELLUS WHOLE; AMARYLLIS BELLADONNA WHOLE; BOS TAURUS EYE; BRYONIA ALBA ROOT; PHOSPHORUS
Active strength: 2; 2; 3; 3; 3; 5; 6; 6; 6; 12; 12 [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
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	63083-2074-2	`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	63083-2074-2	`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	63083-2074-2	`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	63083-2074-2	`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	63083-2074-2	`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	63083-2074-2	`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	63083-2074-2	`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	63083-2074-2	`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	63083-2074-2	`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	63083-2074-2	`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	63083-2074-2	`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	63083-2074-2	`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	63083-2074-2	`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	63083-2074-2	`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	63083-2074-2	`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: Glaucoma Drops
Brand name suffix: 2074
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
PLECTRANTHUS BARBATUS ROOT OIL	2 [hp_X]/59mL
BILBERRY	2 [hp_X]/59mL
EUPHRASIA STRICTA	3 [hp_X]/59mL
GELSEMIUM SEMPERVIRENS ROOT	3 [hp_X]/59mL
SPIGELIA ANTHELMIA WHOLE	3 [hp_X]/59mL
GOLDENSEAL	5 [hp_X]/59mL
ACONITUM NAPELLUS WHOLE	6 [hp_X]/59mL
AMARYLLIS BELLADONNA WHOLE	6 [hp_X]/59mL
BOS TAURUS EYE	6 [hp_X]/59mL
BRYONIA ALBA ROOT	12 [hp_X]/59mL
PHOSPHORUS	12 [hp_X]/59mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 11 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
5NXR7DJ9WO	Internal UNII lookup
9P2U39H18W	Internal UNII lookup
C9642I91WL	Internal UNII lookup
639KR60Q1Q	Internal UNII lookup
WYT05213GE	Internal UNII lookup
ZW3Z11D0JV	Internal UNII lookup
U0NQ8555JD	Internal UNII lookup
11B89M58UN	Internal UNII lookup
VTW461N43P	Internal UNII lookup
T7J046YI2B	Internal UNII lookup
27YLU75U4W	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
7cf2052e-15f8-4b04-ae18-1847da8f4236	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
Effective	Related label
2026-01-09	C74
2026-01-09	C74
2024-01-30	C74
2024-01-30	C74

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
63083-2074-2	Glaucoma Drops2074	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
63083-2074	GLAUCOMA DROPS 2074 (GLAUCOMA DROPS) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]	1	Current NDC, Legacy NDC, 1 package rows	20220215_7cf2052e-15f8-4b04-ae18-1847da8f4236.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
Glaucoma Drops 2074	GLAUCOMA DROPS	Professional Complementary Health Formulas	7cf2052e-15f8-4b04-ae18-1847da8f4236	2026-01-08	Warnings	Exact identifier ndc (product): 63083-2074

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
5NXR7DJ9WO	PLECTRANTHUS BARBATUS ROOT OIL		PLECTRANTHUS BARBATUS ROOT OIL
9P2U39H18W	BILBERRY		BILBERRY
C9642I91WL	EUPHRASIA STRICTA		EUPHRASIA STRICTA
639KR60Q1Q	GELSEMIUM SEMPERVIRENS ROOT		GELSEMIUM SEMPERVIRENS ROOT
ZW3Z11D0JV	GOLDENSEAL		GOLDENSEAL
11B89M58UN	AMARYLLIS BELLADONNA WHOLE		AMARYLLIS BELLADONNA WHOLE
VTW461N43P	BOS TAURUS EYE		BOS TAURUS EYE
T7J046YI2B	BRYONIA ALBA ROOT		BRYONIA ALBA ROOT
27YLU75U4W	PHOSPHORUS	7723-14-0	PHOSPHORUS

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
63083-2074-2	63083207402	59 mL in 1 BOTTLE, DROPPER (63083-2074-2)	59 ml	1985-08-15	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
C74	Professional Complementary Health Formulas \| Natural Pharmaceutical Manufacturing LLC	2026-01-08	HUMAN OTC DRUG LABEL	2