Home NDC 69842-330 Witch Hazel
Product NDC 69842-330
11-digit product format 698420330
Labeler code 69842
Product ID 69842-330_471acbcb-03ea-43fd-e063-6394a90a1294
Type HUMAN OTC DRUG
Nonproprietary name WITCH HAZEL
Dosage form LIQUID
Route TOPICAL
Labeler CVS HEALTH
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-02-24
Marketing end 2026-10-31
Substance WITCH HAZEL
Active strength 84 g/100mL
NDC exclude flag No
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 Active Ingredients# Ingredient, Strength table Ingredient Strength WITCH HAZEL 84 g/100mL
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 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 69842-330-16 Witch Hazel 473 mL in 1 BOTTLE LIQUID 473 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69842-330 WITCH HAZEL LIQUID [CVS HEALTH] 4 Current NDC, 1 package rows 20241213_b8b79e8d-9c84-1700-e053-2995a90af5bd.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 48 of 153 · 3,057 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 69842-330-16 69842033016 473 mL in 1 BOTTLE (69842-330-16) 473 ml 2023-02-24 2026-10-31 No No Historical