witch hazel
Generic: witch hazel
Labeler: cvs pharmacy, inc.Drug Facts
Product Profile
Brand Name
witch hazel
Generic Name
witch hazel
Labeler
cvs pharmacy, inc.
Dosage Form
LIQUID
Routes
Active Ingredients
witch hazel 860 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
59779-045
Product ID
59779-045_49ed94e0-a9d0-ca73-e063-6394a90a8a51
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M015
Listing Expiration
2027-12-31
Marketing Start
2011-04-04
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
59779045
Hyphenated Format
59779-045
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
M015 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 860 mg/mL
Packaging
- 473 mL in 1 BOTTLE, PLASTIC (59779-045-43)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "49ed94e0-a9d0-ca73-e063-6394a90a8a51", "openfda": {"unii": ["101I4J0U34"], "rxcui": ["200295"], "spl_set_id": ["50f920da-b41a-480d-b3a0-df940caaee2d"], "manufacturer_name": ["CVS Pharmacy, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE, PLASTIC (59779-045-43)", "package_ndc": "59779-045-43", "marketing_start_date": "20110404"}], "brand_name": "Witch Hazel", "product_id": "59779-045_49ed94e0-a9d0-ca73-e063-6394a90a8a51", "dosage_form": "LIQUID", "product_ndc": "59779-045", "generic_name": "Witch Hazel", "labeler_name": "CVS Pharmacy, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Witch Hazel", "active_ingredients": [{"name": "WITCH HAZEL", "strength": "860 mg/mL"}], "application_number": "M015", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20110404", "listing_expiration_date": "20271231"}