Home NDC 37808-757 HEB A.C. Eye Drops
Product NDC 37808-757
11-digit product format 378080757
Labeler code 37808
Product ID 37808-757_0cfaa641-21fd-e11b-e063-6394a90a69f2
Type HUMAN OTC DRUG
Nonproprietary name tetrahydrozoline HCl, zinc sulfate
Dosage form SOLUTION
Route OPHTHALMIC
Labeler HEB Grocery Company., LP
Application M018
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-03-23
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 HEB A.C. Eye Drops
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.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 37808-757-01 HEB A.C. Eye Drops 1 in 1 CARTON SOLUTION 1 2 37808-757-01 HEB A.C. Eye Drops 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 37808-757 HEB A.C. EYE DROPS (TETRAHYDROZOLINE HCL, ZINC SULFATE) SOLUTION [HEB GROCERY COMPANY., LP] 2 Current NDC, 2 package rows 20231221_f680a8c1-dc91-7a52-e053-2a95a90a571e.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 6 of 25 · 494 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 37808-757-01 37808075701 1 BOTTLE, DROPPER in 1 CARTON (37808-757-01) / 15 mL in 1 BOTTLE, DROPPER 2023-03-23 No No Current