Witch Hazel

Product NDC
79481-0617
11-digit product format
794810617
Labeler code
79481
Product ID
79481-0617_42784a86-d834-e49c-e063-6394a90ac9ac
Type
HUMAN OTC DRUG
Nonproprietary name
Witch Hazel
Dosage form
SPRAY
Route
TOPICAL
Labeler
Meijer Distribution 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

Additional Listing Data#

Finished product
Yes
Brand name base
Witch Hazel
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
WITCH HAZEL860 mg/g

Harmonized Identifiers#

Field, Values table
FieldValues
Unii101I4J0U34
Rxcui1987674

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79481-0617-1Witch Hazel170 g in 1 CANSPRAY1704

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79481-0617WITCH HAZEL SPRAY [MEIJER DISTRIBUTION INC]3Current NDC, 1 package rows20241016_03f23b04-e7f7-49b7-e063-6294a90ad58a.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1987674witch hazel 86 % Topical SprayPSN03f23b04-e7f7-49b7-e063-6294a90ad58a4
1987674witch hazel 860 MG/ML Topical SpraySCD03f23b04-e7f7-49b7-e063-6294a90ad58a4
1987674witch hazel 86 % Topical SpraySY03f23b04-e7f7-49b7-e063-6294a90ad58a4

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
79481-0617-179481061701170 g in 1 CAN (79481-0617-1) 170 g2023-08-27NoNoCurrent