gnp witch hazel
Generic: witch hazel
Labeler: amerisource bergenDrug Facts
Product Profile
Brand Name
gnp witch hazel
Generic Name
witch hazel
Labeler
amerisource bergen
Dosage Form
LIQUID
Routes
Active Ingredients
witch hazel 855 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
46122-335
Product ID
46122-335_0c82455f-5208-fa88-e063-6294a90a2518
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M016
Listing Expiration
2026-12-31
Marketing Start
2016-01-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
46122335
Hyphenated Format
46122-335
Supplemental Identifiers
UPC
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
gnp witch hazel (source: ndc)
Generic Name
witch hazel (source: ndc)
Application Number
M016 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 855 mg/mL
Packaging
- 473 mL in 1 BOTTLE (46122-335-43)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "0c82455f-5208-fa88-e063-6294a90a2518", "openfda": {"upc": ["0087701427336"], "unii": ["101I4J0U34"], "spl_set_id": ["45ac839d-215d-4c5f-8ae5-5e111d170061"], "manufacturer_name": ["Amerisource Bergen"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (46122-335-43)", "package_ndc": "46122-335-43", "marketing_start_date": "20160101"}], "brand_name": "GNP Witch Hazel", "product_id": "46122-335_0c82455f-5208-fa88-e063-6294a90a2518", "dosage_form": "LIQUID", "product_ndc": "46122-335", "generic_name": "Witch Hazel", "labeler_name": "Amerisource Bergen", "product_type": "HUMAN OTC DRUG", "brand_name_base": "GNP Witch Hazel", "active_ingredients": [{"name": "WITCH HAZEL", "strength": "855 mg/mL"}], "application_number": "M016", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20160101", "listing_expiration_date": "20261231"}