Home NDC 59640-218 CLEAR ANTI ITCH
Product NDC 59640-218
11-digit product format 596400218
Labeler code 59640
Product ID 59640-218_54f04056-d806-8c62-e063-6394a90ab740
Type HUMAN OTC DRUG
Nonproprietary name pramoxine hcl, zinc acetate lotion
Dosage form LOTION
Route TOPICAL
Labeler H E B
Application M016
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-06-23
Substance PRAMOXINE HCL; ZINC ACETATE
Active strength 10; 1 mg/mL; mg/mL
Pharmacologic classes Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
NDC exclude flag No
Listing certified through 2027-12-31
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 CLEAR ANTI ITCH
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PRAMOXINE HCL 10 mg/mL ZINC ACETATE 1 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 88AYB867L5 Internal UNII lookup FM5526K07A Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1234546 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 39 of 68 · 1,357 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 59640-218-30 59640021830 177 mL in 1 BOTTLE, PLASTIC (59640-218-30) 177 ml 2026-06-23 No No Current