medicated pads
Generic: witch hazel
Labeler: target corporationDrug Facts
Product Profile
Brand Name
medicated pads
Generic Name
witch hazel
Labeler
target corporation
Dosage Form
PATCH
Routes
Active Ingredients
witch hazel 50 mg/100mg
Manufacturer
Identifiers & Regulatory
Product NDC
11673-614
Product ID
11673-614_412203ce-d7fc-28ee-e063-6394a90a929f
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M015
Listing Expiration
2026-12-31
Marketing Start
2020-05-15
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
11673614
Hyphenated Format
11673-614
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
medicated pads (source: ndc)
Generic Name
witch hazel (source: ndc)
Application Number
M015 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/100mg
Packaging
- 100 PATCH in 1 BOX (11673-614-10) / 50 mg in 1 PATCH
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "412203ce-d7fc-28ee-e063-6394a90a929f", "openfda": {"unii": ["101I4J0U34"], "rxcui": ["844379"], "spl_set_id": ["acd0d99d-2a77-4227-bebb-c819f4a52666"], "manufacturer_name": ["TARGET CORPORATION"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 PATCH in 1 BOX (11673-614-10) / 50 mg in 1 PATCH", "package_ndc": "11673-614-10", "marketing_start_date": "20200515"}], "brand_name": "medicated pads", "product_id": "11673-614_412203ce-d7fc-28ee-e063-6394a90a929f", "dosage_form": "PATCH", "product_ndc": "11673-614", "generic_name": "Witch Hazel", "labeler_name": "TARGET CORPORATION", "product_type": "HUMAN OTC DRUG", "brand_name_base": "medicated pads", "active_ingredients": [{"name": "WITCH HAZEL", "strength": "50 mg/100mg"}], "application_number": "M015", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200515", "listing_expiration_date": "20261231"}