prestige
Generic: chloroxylenol
Labeler: sunburst chemicals, inc.Drug Facts
Product Profile
Brand Name
prestige
Generic Name
chloroxylenol
Labeler
sunburst chemicals, inc.
Dosage Form
SOAP
Routes
Active Ingredients
chloroxylenol 10 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
63621-335
Product ID
63621-335_14308390-5ca6-80b4-e063-6294a90a02ee
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2026-12-31
Marketing Start
2020-04-03
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63621335
Hyphenated Format
63621-335
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
prestige (source: ndc)
Generic Name
chloroxylenol (source: ndc)
Application Number
505G(a)(3) (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/mL
Packaging
- 3785 mL in 1 BOTTLE, PLASTIC (63621-335-14)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "14308390-5ca6-80b4-e063-6294a90a02ee", "openfda": {"unii": ["0F32U78V2Q"], "rxcui": ["413257"], "spl_set_id": ["2e4bb97c-9c16-43d1-aea3-54723c7afc45"], "manufacturer_name": ["Sunburst Chemicals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3785 mL in 1 BOTTLE, PLASTIC (63621-335-14)", "package_ndc": "63621-335-14", "marketing_start_date": "20200403"}], "brand_name": "Prestige", "product_id": "63621-335_14308390-5ca6-80b4-e063-6294a90a02ee", "dosage_form": "SOAP", "product_ndc": "63621-335", "generic_name": "Chloroxylenol", "labeler_name": "Sunburst Chemicals, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Prestige", "active_ingredients": [{"name": "CHLOROXYLENOL", "strength": "10 mg/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200403", "listing_expiration_date": "20261231"}