Equaline Eye Drops A.C.

Product NDC: 41163-540
11-digit product format: 411630540
Labeler code: 41163
Product ID: 41163-540_0cfac3c3-6f4a-cc70-e063-6394a90a57b1
Type: HUMAN OTC DRUG
Nonproprietary name: tetrahydrozoline HCl, zinc sulfate
Dosage form: SOLUTION
Route: OPHTHALMIC
Labeler: United Natural Foods, Inc.
Application: M018
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2023-03-22
Substance: TETRAHYDROZOLINE HYDROCHLORIDE; ZINC SULFATE
Active strength: .05; .25 g/100mL; g/100mL
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: Equaline Eye Drops A.C.
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
TETRAHYDROZOLINE HYDROCHLORIDE	.05 g/100mL
ZINC SULFATE	.25 g/100mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
0YZT43HS7D	Internal UNII lookup
89DS0H96TB	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
f5f894f0-1ab0-4cad-e053-2995a90a7cba	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
777d68c6-a5ab-e06c-d314-677b0b9af0c8	Product name	2	20240508
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
41163-540-01	Equaline Eye Drops A.C.	1 in 1 CARTON	SOLUTION	1		2
41163-540-01	Equaline Eye Drops A.C.	15 mL in 1 BOTTLE, DROPPER	SOLUTION	15		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
41163-540	EQUALINE EYE DROPS A.C. (TETRAHYDROZOLINE HCL, ZINC SULFATE) SOLUTION [UNITED NATURAL FOODS, INC.]	2	Current NDC, 2 package rows	20231224_f5f894f0-1ab0-4cad-e053-2995a90a7cba.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 22 of 25 · 494 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Meijer Maximum Redness Relief and Lubricant	GLYCERIN, NAPHAZOLINE HCI	Meijer Distribution, Inc.	9feb1818-c79b-23bf-e053-2995a90a1084	2023-12-22	Warnings	Exact identifier application number: M018
Meijer Redness Relief	TETRAHYDROZOLINE HCI	Meijer Distribution, Inc.	9fea27a5-b81b-1598-e053-2995a90a6b62	2023-12-22	Warnings	Exact identifier application number: M018
Meijer Seasonal Itching and Redness Relief	TETRAHYDROZOLINE HCI, ZINC SULFATE	Meijer Distribution, Inc.	9fead2de-2fe6-4dab-e053-2995a90a2742	2023-12-22	Warnings	Exact identifier application number: M018
Meijer Artificial Tears	POLYVINYL ALCOHOL, POVIDONE	Meijer Distribution, Inc.	9feb3eec-a36f-8fc7-e053-2a95a90adcd3	2023-12-22	Warnings	Exact identifier application number: M018
Meijer Redness Relief	GLYCERIN, NAPHAZOLINE HCI	Meijer Distribution, Inc.	9fea4e43-7525-bb66-e053-2a95a90acee9	2023-12-22	Warnings	Exact identifier application number: M018
Meijer Ultra Lubricant Eye Drops High Performance	POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL	Meijer Distribution, Inc.	a0846e3e-687c-fd55-e053-2995a90a673e	2023-12-22	Warnings	Exact identifier application number: M018
Meijer Advanced Redness and Irritation Relief	DEXTRAN 70, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HCI	Meijer Distribution, Inc.	9fea6d7a-a2cd-d26e-e053-2995a90a15f8	2023-12-22	Warnings	Exact identifier application number: M018
Meijer Dry Eye Relief	GLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400	Meijer Distribution, Inc.	9feaa5e2-6aca-96e8-e053-2a95a90a54bd	2023-12-22	Warnings	Exact identifier application number: M018
Walgreens Multi-Symptom Relief Eye Drops	GLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400, TETRAHYDROZOLINE HCL, ZINC SULFATE	Walgreen Co.	a03789ce-66bd-7b12-e053-2995a90af85a	2023-12-20	Warnings	Exact identifier application number: M018
Walgreens Lubricant Eye Drops Preservative Free	DEXTRAN 70, HYPROMELLOSE	Walgreen Company	9b383e41-e116-1c12-e053-2a95a90ab25f	2023-12-20	Warnings	Exact identifier application number: M018
Walgreens Eye Drops Maximum Redness Relief 15mL	GLYCERIN, NAPHAZOLINE HCI	Walgreen Company	949d4a4d-b0f8-81f8-e053-2995a90a818d	2023-12-20	Warnings	Exact identifier application number: M018
Walgreens Eye Drops Seasonal Relief 15mL	TETRAHYDROZOLINE HCI, ZINC SULFATE	Walgreen Co.	947f3706-ef5e-2c53-e053-2a95a90a82bd	2023-12-20	Warnings	Exact identifier application number: M018
Walgreens Eye Drops Advanced Relief 15mL	DEXTRAN 70, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HCI	Walgreen Company	949f5560-fba7-2da8-e053-2995a90a23c2	2023-12-20	Warnings	Exact identifier application number: M018
Walgreens Lubricant Eye Drops Preservative Free	CARBOXYMETHYLCELLULOSE SODIUM	Walgreen Company	9912b773-e7a5-3a82-e053-2995a90a5b2c	2023-12-20	Warnings	Exact identifier application number: M018
Walgreens Lubricant Eye Drops High Performance 15mL and twin pack	POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL	Walgreen Company	94ee8310-1c19-dfd4-e053-2a95a90a8356	2023-12-20	Warnings	Exact identifier application number: M018
Walgreens Redness Relief Eye Drops 15mL	GLYCERIN, NAPHAZOLINE HCI	Walgreen Company	94a0d08a-a6db-1088-e053-2995a90ab4fd	2023-12-20	Warnings	Exact identifier application number: M018
Walgreens Eye Drops Original 15mL and twin pack	TETRAHYDROZOLINE HCI	Walgreens Company	94e391f7-db4b-47d2-e053-2a95a90a1b11	2023-12-20	Warnings	Exact identifier application number: M018
Walgreens Lubricant Eye Drops Dry Eye 15mL and twin pack	POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL	Walgreen Company	94f6e1cd-073c-61ca-e053-2a95a90ae725	2023-12-20	Warnings	Exact identifier application number: M018
Lubricant Eye Drops Preservative Free	CARBOXYMETHYLCELLULOSE SODIUM	Target Corporation	454ce049-49e5-48b1-8499-048e5e7d72d3	2023-12-20	Warnings	Exact identifier application number: M018
Rugby Lubricant Eye Drops	CARBOXYMETHYLCELLULOSE SODIUM	Rugby Laboratories	f9292d5d-e0a3-9287-e053-6294a90a43e9	2023-12-20	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	f5f894f0-1ab0-4cad-e053-2995a90a7cba	2
1043249	tetrahydrozoline hydrochloride 0.5 MG/ML / zinc sulfate 2.5 MG/ML Ophthalmic Solution	SCD	f5f894f0-1ab0-4cad-e053-2995a90a7cba	2
1043249	tetrahydrozoline HCl 0.05 % / zinc sulfate 0.25 % Ophthalmic Solution	SY	f5f894f0-1ab0-4cad-e053-2995a90a7cba	2
1043249	Tetrahydrozoline hydrochloride 0.5 MG/ML / ZnSO4 2.5 MG/ML Ophthalmic Solution	SY	f5f894f0-1ab0-4cad-e053-2995a90a7cba	2

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Sample	Exclude flag	Status
41163-540-01	41163054001	1 BOTTLE, DROPPER in 1 CARTON (41163-540-01) / 15 mL in 1 BOTTLE, DROPPER	2023-03-22	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Equaline Eye Drops A.C.15 mL (PLD)	United Natural Foods, Inc. \| KC Pharmaceuticals, Inc. \| K.C. Pharmaceuticals, Inc.	2023-12-20	HUMAN OTC DRUG LABEL	2