Home NDC 11344-822 Witch Hazel
Product NDC 11344-822
11-digit product format 113440822
Labeler code 11344
Product ID 11344-822_5b85ae92-95a0-47ff-e063-6394a90a0156
Type HUMAN OTC DRUG
Nonproprietary name Witch Hazel
Dosage form LIQUID
Route TOPICAL
Labeler Nice-Pak Products, LLC
Application M016
Marketing category OTC MONOGRAPH DRUG
Marketing start 1998-01-29
Substance WITCH HAZEL
Active strength 860 mg/mL
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 Witch Hazel
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength WITCH HAZEL 860 mg/mL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 11344-822-43 Witch Hazel 473 mL in 1 BOTTLE, PLASTIC LIQUID 473 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 11344-822 WITCH HAZEL LIQUID [CONSUMER PRODUCT PARTNERS, LLC] 2 Current NDC, 1 package rows 20250302_f1e68ec8-f269-40c8-863f-69290812feed.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 39 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 11344-822-43 11344082243 473 mL in 1 BOTTLE, PLASTIC (11344-822-43) 473 ml 1998-01-29 No No Current