humco witch hazel
Generic: witch hazel
Labeler: humco holding group, inc.Drug Facts
Product Profile
Brand Name
humco witch hazel
Generic Name
witch hazel
Labeler
humco holding group, inc.
Dosage Form
LIQUID
Routes
Active Ingredients
witch hazel 884 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0395-3213
Product ID
0395-3213_0c936cb3-838f-0603-e063-6394a90a0640
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M016
Listing Expiration
2026-12-31
Marketing Start
2012-02-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
03953213
Hyphenated Format
0395-3213
Supplemental Identifiers
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
humco witch hazel (source: ndc)
Generic Name
witch hazel (source: ndc)
Application Number
M016 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 884 mg/mL
Packaging
- 473 mL in 1 BOTTLE (0395-3213-16)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "0c936cb3-838f-0603-e063-6394a90a0640", "openfda": {"unii": ["101I4J0U34"], "spl_set_id": ["3cf07016-a129-49ca-8fad-b67dda5aa009"], "manufacturer_name": ["Humco Holding Group, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (0395-3213-16)", "package_ndc": "0395-3213-16", "marketing_start_date": "20120201"}], "brand_name": "Humco Witch Hazel", "product_id": "0395-3213_0c936cb3-838f-0603-e063-6394a90a0640", "dosage_form": "LIQUID", "product_ndc": "0395-3213", "generic_name": "Witch Hazel", "labeler_name": "Humco Holding Group, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Humco Witch Hazel", "active_ingredients": [{"name": "WITCH HAZEL", "strength": "884 mg/mL"}], "application_number": "M016", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20120201", "listing_expiration_date": "20261231"}