Home NDC 56104-904 Witch Hazel
Product NDC 56104-904
11-digit product format 561040904
Labeler code 56104
Product ID 56104-904_42b885ee-203a-2e7a-e063-6394a90ad29b
Type HUMAN OTC DRUG
Nonproprietary name Witch Hazel
Dosage form SPRAY
Route TOPICAL
Labeler Premier Brands of America Inc.
Application M016
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-08-27
Substance WITCH HAZEL
Active strength 860 mg/g
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 Witch Hazel
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength WITCH HAZEL 860 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 101I4J0U34 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1987674 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 56104-904-01 Witch Hazel 170 g in 1 CAN SPRAY 170 2
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 44 of 68 · 1,357 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 56104-904-01 56104090401 170 g in 1 CAN (56104-904-01) 170 g 2025-06-23 No No Current