Home NDC 79948-412 Oilogic Prego Witch Hazel Cooling
Product NDC 79948-412
11-digit product format 799480412
Labeler code 79948
Product ID 79948-412_557e526c-347d-1463-e063-6394a90a8628
Type HUMAN OTC DRUG
Nonproprietary name Witch Hazel
Dosage form SPRAY
Route TOPICAL
Labeler Ignite Brands LLC
Application M016
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-11-01
Substance WITCH HAZEL
Active strength 50 g/100g
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 Oilogic Prego Witch Hazel Cooling
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength WITCH HAZEL 50 g/100g
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 2755463 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 44 of 67 · 1,323 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 79948-412-04 79948041204 116.82 g in 1 BOTTLE (79948-412-04) 116.82 g 2026-11-01 No No Current