witch hazel
Generic: witch hazel
Labeler: hydrox laboratoriesDrug Facts
Product Profile
Brand Name
witch hazel
Generic Name
witch hazel
Labeler
hydrox laboratories
Dosage Form
LIQUID
Routes
Active Ingredients
witch hazel 86 g/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
10565-040
Product ID
10565-040_48334703-dd80-8848-e063-6294a90a2cb9
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2027-12-31
Marketing Start
2011-12-21
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
10565040
Hyphenated Format
10565-040
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
witch hazel (source: ndc)
Generic Name
witch hazel (source: ndc)
Application Number
505G(a)(3) (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 86 g/100mL
Packaging
- 473 mL in 1 BOTTLE, PLASTIC (10565-040-16)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "48334703-dd80-8848-e063-6294a90a2cb9", "openfda": {"unii": ["101I4J0U34"], "rxcui": ["200295"], "spl_set_id": ["73391eb3-c17c-4104-93b1-2decfb2ebdf9"], "manufacturer_name": ["Hydrox Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE, PLASTIC (10565-040-16)", "package_ndc": "10565-040-16", "marketing_start_date": "20171113"}], "brand_name": "Witch Hazel", "product_id": "10565-040_48334703-dd80-8848-e063-6294a90a2cb9", "dosage_form": "LIQUID", "product_ndc": "10565-040", "generic_name": "Witch Hazel", "labeler_name": "Hydrox Laboratories", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Witch Hazel", "active_ingredients": [{"name": "WITCH HAZEL", "strength": "86 g/100mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20111221", "listing_expiration_date": "20271231"}