Medics Choice Eye Drops Seasonal Relief

Product NDC: 55651-024
11-digit product format: 556510024
Labeler code: 55651
Product ID: 55651-024_4748cbbd-a95a-77cf-e063-6294a90a92b5
Type: HUMAN OTC DRUG
Nonproprietary name: tetrahydrozoline hydrochloride, zinc sulfate
Dosage form: SOLUTION/ DROPS
Route: OPHTHALMIC
Labeler: KC Pharmaceuticals, Inc.
Application: M018
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2003-10-23
Substance: ZINC SULFATE; TETRAHYDROZOLINE HYDROCHLORIDE
Active strength: 2.5; .5 mg/mL; mg/mL
Pharmacologic classes: Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

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: Medics Choice Eye Drops Seasonal Relief
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ZINC SULFATE	2.5 mg/mL
TETRAHYDROZOLINE HYDROCHLORIDE	.5 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
89DS0H96TB	Internal UNII lookup
0YZT43HS7D	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1043249	Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
Identifier	FDA.report destination
92bd8cb4-90ad-4a47-afa4-30d1fa658d62	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
f47a510b-6679-4664-b2d6-47b5c4afe7cc	Product name	4	20260217
030ce964-9b2d-45aa-b5d3-f78ce03ef61c	Product name	2	20250515
777d68c6-a5ab-e06c-d314-677b0b9af0c8	Product name	2	20240508
0306390c-dd77-4363-afe0-63c58088b2a1	Product name	1	20220120
503ea967-4b9c-48cf-9e87-c7975295849d	Product name	2	20220120
d5e51f11-ad28-caa4-4b49-4143974782ad	Product name	1	20150831
190f2a5b-bbc8-65c7-fcb0-97891307b917	Product name	1	20140508
27945931-b6e2-158e-d615-4ef21e2af974	Product name	1	20140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
55651-024-01	Medics Choice Eye Drops Seasonal Relief	1 in 1 CARTON	SOLUTION/ DROPS	1		6
55651-024-01	Medics Choice Eye Drops Seasonal Relief	15 mL in 1 BOTTLE, DROPPER	SOLUTION/ DROPS	15		6

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
TETRAHYDROZOLINE HYDROCHLORIDE	ACTIVE INGREDIENT	0YZT43HS7D	EYE DROPS AC (TETRAHYDROZOLINE HYDROCHLORIDE, ZINC SULFATE) SOLUTION/ DROPS [KC PHARMACEUTICALS, INC.]	1
ZINC SULFATE	ACTIVE INGREDIENT	89DS0H96TB	EYE DROPS AC (TETRAHYDROZOLINE HYDROCHLORIDE, ZINC SULFATE) SOLUTION/ DROPS [KC PHARMACEUTICALS, INC.]	1
TETRAHYDROZOLINE	ACTIVE MOIETY	S9U025Y077	EYE DROPS AC (TETRAHYDROZOLINE HYDROCHLORIDE, ZINC SULFATE) SOLUTION/ DROPS [KC PHARMACEUTICALS, INC.]	1
ZINC	ACTIVE MOIETY	J41CSQ7QDS	EYE DROPS AC (TETRAHYDROZOLINE HYDROCHLORIDE, ZINC SULFATE) SOLUTION/ DROPS [KC PHARMACEUTICALS, INC.]	1
BENZALKONIUM CHLORIDE	INACTIVE INGREDIENT	F5UM2KM3W7	EYE DROPS AC (TETRAHYDROZOLINE HYDROCHLORIDE, ZINC SULFATE) SOLUTION/ DROPS [KC PHARMACEUTICALS, INC.]	1
BORIC ACID	INACTIVE INGREDIENT	R57ZHV85D4	EYE DROPS AC (TETRAHYDROZOLINE HYDROCHLORIDE, ZINC SULFATE) SOLUTION/ DROPS [KC PHARMACEUTICALS, INC.]	1
EDETATE DISODIUM	INACTIVE INGREDIENT	7FLD91C86K	EYE DROPS AC (TETRAHYDROZOLINE HYDROCHLORIDE, ZINC SULFATE) SOLUTION/ DROPS [KC PHARMACEUTICALS, INC.]	1
SODIUM CHLORIDE	INACTIVE INGREDIENT	451W47IQ8X	EYE DROPS AC (TETRAHYDROZOLINE HYDROCHLORIDE, ZINC SULFATE) SOLUTION/ DROPS [KC PHARMACEUTICALS, INC.]	1
SODIUM CITRATE	INACTIVE INGREDIENT	1Q73Q2JULR	EYE DROPS AC (TETRAHYDROZOLINE HYDROCHLORIDE, ZINC SULFATE) SOLUTION/ DROPS [KC PHARMACEUTICALS, INC.]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	EYE DROPS AC (TETRAHYDROZOLINE HYDROCHLORIDE, ZINC SULFATE) SOLUTION/ DROPS [KC PHARMACEUTICALS, INC.]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
55651-024	MEDICS CHOICE EYE DROPS SEASONAL RELIEF (TETRAHYDROZOLINE HYDROCHLORIDE, ZINC SULFATE) SOLUTION/ DROPS [KC PHARMACEUTICALS, INC.]	5	Current NDC, Legacy NDC, 2 package rows	20240110_92bd8cb4-90ad-4a47-afa4-30d1fa658d62.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 19 of 25 · 494 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Eye Wash	WATER	Hubei Changjian Medical Products Co., Ltd.	d57e1c5b-1edc-4a94-88bc-f9ecf347b7ea	2024-10-11	Warnings	Exact identifier application number: M018
Capasil Pain Relieving	MENTHOL, METHYL SALICYLATE	PureTek Corporation	b1a8e78c-57f0-1f3e-e053-2995a90acbd5	2024-10-01	Warnings	Exact identifier application number: M018
Mencylate Pain Relieving	MENTHOL, METHYL SALICYLATE	PureTek Corporation	f824de86-9492-2e6b-e053-6294a90a6f2a	2024-10-01	Warnings	Exact identifier application number: M018
Advanced Eye Relief/ Redness Maximum Relief	NAPHAZOLINE HYDROCHLORIDE AND HYPROMELLOSE	Bausch & Lomb Incorporated	3c11285a-7e86-4b47-b1ee-e7d59858087d	2024-09-25	Warnings	Exact identifier application number: M018
Muro 128	SODIUM CHLORIDE	Bausch & Lomb Incorporated	cc3d5bc8-9d3c-4c65-9e43-707a2db4081a	2024-09-25	Warnings	Exact identifier application number: M018
Muro 128	SODIUM CHLORIDE	Bausch & Lomb Incorporated	93fafa27-5031-4d95-b4b8-5574b7204ae2	2024-09-25	Warnings	Exact identifier application number: M018
Muro 128	SODIUM CHLORIDE	Bausch & Lomb Incorporated	454f337e-d897-46de-ab05-1c543a33061c	2024-09-25	Warnings	Exact identifier application number: M018
PURPOSE	OCTINOXATE, OCTISALATE AND OXYBENZONE	Bausch & Lomb Incorporated	a1e14135-b8da-4cee-8c5b-1893572f4de4	2024-09-25	Warnings	Exact identifier application number: M018
Soothe Night Time	WHITE PETROLATUM MINERAL OIL	Bausch & Lomb Incorporated	638d3c3f-9960-43da-956e-0e28c77f533e	2024-09-24	Warnings	Exact identifier application number: M018
blink tears	POLYETHYLENE GLYCOL 400	Bausch & Lomb Incorporated	10fcf407-6eaf-4730-9ed0-9b7715cf5701	2024-09-20	Warnings	Exact identifier application number: M018
Soothe XP Preservative Free	LIGHT MINERAL OIL AND MINERAL OIL	Bausch & Lomb Incorporated	b254d885-6d49-4c95-b6be-cfdad49c85e6	2024-09-20	Warnings	Exact identifier application number: M018
blink gel tears	POLYETHYLENE GLYCOL 400	Bausch & Lomb Incorporated	6f7e06c3-204d-459a-af8f-c46be9ad0e8d	2024-09-20	Warnings	Exact identifier application number: M018
Soothe XP	LIGHT MINERAL OIL AND MINERAL OIL	Bausch & Lomb Incorporated	c0f053da-8d22-433e-a36e-79cf15ad387f	2024-09-20	Warnings	Exact identifier application number: M018
Soothe	GLYCERIN AND PROPYLENE GLYCOL	Bausch & Lomb Incorporated	fef002ea-c4bd-4486-a42e-1bbd9d73d28d	2024-09-20	Warnings	Exact identifier application number: M018
Leader Preservative-Free Ultra Lubricating Eye Drops	POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL	Cardinal Health	2a2aa620-ca63-4698-88fd-fc263b8fa0d1	2024-09-07	Warnings	Exact identifier application number: M018
Eyesaline Emergency Eyewash	PURIFIED WATER	Honeywell Safety Products USA, Inc.	ad42a7e3-84ea-390d-e053-2a95a90a3a32	2024-06-14	Warnings	Exact identifier application number: M018
Artificial Tears	POLYVINYL ALCOHOL, POVIDONE	NuCare Pharmaceuticals,Inc.	9c1c4911-908e-3c3c-e053-2995a90abcfc	2024-06-14	Warnings	Exact identifier application number: M018
Eyes Alive Eye Wash	WATER	RIVIERA PHARMA INC	081079f4-1c06-4054-b771-00fedaa666f6	2024-06-05	Warnings	Exact identifier application number: M018
Eyes Alive Lubricating	CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED	RIVIERA PHARMA INC	b6966691-6884-438c-9f89-5924089226e1	2024-05-31	Warnings	Exact identifier application number: M018
Eye Wash	WATER	M-star (Hubei) Health&Care Products Co., Ltd.	71706039-e250-4f08-9687-71b2928c4e46	2024-04-01	Warnings	Exact identifier application number: M018

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
0YZT43HS7D	TETRAHYDROZOLINE HYDROCHLORIDE	522-48-5	TETRAHYDROZOLINE HYDROCHLORIDE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1043249	tetrahydrozoline HCl 0.05 % / zinc sulfate 0.25 % Ophthalmic Solution	PSN	92bd8cb4-90ad-4a47-afa4-30d1fa658d62	6
1043249	tetrahydrozoline hydrochloride 0.5 MG/ML / zinc sulfate 2.5 MG/ML Ophthalmic Solution	SCD	92bd8cb4-90ad-4a47-afa4-30d1fa658d62	6
1043249	tetrahydrozoline HCl 0.05 % / zinc sulfate 0.25 % Ophthalmic Solution	SY	92bd8cb4-90ad-4a47-afa4-30d1fa658d62	6
1043249	Tetrahydrozoline hydrochloride 0.5 MG/ML / ZnSO4 2.5 MG/ML Ophthalmic Solution	SY	92bd8cb4-90ad-4a47-afa4-30d1fa658d62	6

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
55651-024-01	55651002401	1 BOTTLE, DROPPER in 1 CARTON (55651-024-01) / 15 mL in 1 BOTTLE, DROPPER	2003-10-23	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Medic's Choice Eye Drops Seasonal Relief	KC Pharmaceuticals, Inc.	2025-12-30	HUMAN OTC DRUG LABEL	6