witch hazel
Generic: witch hazel
Labeler: topco associates llcDrug Facts
Product Profile
Brand Name
witch hazel
Generic Name
witch hazel
Labeler
topco associates llc
Dosage Form
LIQUID
Routes
Active Ingredients
witch hazel 860 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
76162-822
Product ID
76162-822_4ab9bfe0-d6b8-9473-e063-6294a90ad884
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M016
Listing Expiration
2027-12-31
Marketing Start
2019-03-08
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
76162822
Hyphenated Format
76162-822
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
M016 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 860 mg/mL
Packaging
- 473 mL in 1 BOTTLE, PLASTIC (76162-822-43)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4ab9bfe0-d6b8-9473-e063-6294a90ad884", "openfda": {"unii": ["101I4J0U34"], "rxcui": ["200295"], "spl_set_id": ["471a9f8d-ba12-41d3-a510-20c1a13ff850"], "manufacturer_name": ["Topco Associates LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE, PLASTIC (76162-822-43)", "package_ndc": "76162-822-43", "marketing_start_date": "20190308"}], "brand_name": "Witch Hazel", "product_id": "76162-822_4ab9bfe0-d6b8-9473-e063-6294a90ad884", "dosage_form": "LIQUID", "product_ndc": "76162-822", "generic_name": "WITCH HAZEL", "labeler_name": "Topco Associates LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Witch Hazel", "active_ingredients": [{"name": "WITCH HAZEL", "strength": "860 mg/mL"}], "application_number": "M016", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190308", "listing_expiration_date": "20271231"}