Witch Hazel

Product NDC
11673-822
11-digit product format
116730822
Labeler code
11673
Product ID
11673-822_b7b722bf-281e-47f8-a0bb-19fe8d6f0ff3
Type
HUMAN OTC DRUG
Nonproprietary name
WITCH HAZEL
Dosage form
LIQUID
Route
TOPICAL
Labeler
Target Corporation
Application
part347
Marketing category
OTC MONOGRAPH FINAL
Marketing start
1998-01-29
Marketing end
0000-00-00
Substance
WITCH HAZEL
Active strength
86 kg/100L
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
WITCH HAZELACTIVE INGREDIENT101I4J0U34WITCH HAZEL LIQUID [TARGET CORPORATION]1
WITCH HAZELACTIVE MOIETY101I4J0U34WITCH HAZEL LIQUID [TARGET CORPORATION]1
ALCOHOLINACTIVE INGREDIENT3K9958V90MWITCH HAZEL LIQUID [TARGET CORPORATION]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11673-822WITCH HAZEL LIQUID [TARGET CORPORATION]16Legacy NDC20240726_62f15711-1f75-446d-bdd4-881b40e3eeab.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
11673-822-4311673082243473 L in 1 BOTTLE, PLASTIC (11673-822-43) 473 l1998-01-290000-00-00NoNoCurrent