chloroxylenol 0.30 %
Generic: chloroxylenol
Labeler: davion, incDrug Facts
Product Profile
Brand Name
chloroxylenol 0.30 %
Generic Name
chloroxylenol
Labeler
davion, inc
Dosage Form
LIQUID
Routes
Active Ingredients
chloroxylenol 3 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
42669-028
Product ID
42669-028_40941cb8-9e8f-44bb-857d-051ec271f213
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2026-12-31
Marketing Start
2025-02-15
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
42669028
Hyphenated Format
42669-028
Supplemental Identifiers
RxCUI
UPC
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
chloroxylenol 0.30 % (source: ndc)
Generic Name
chloroxylenol (source: ndc)
Application Number
505G(a)(3) (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 3 mg/mL
Packaging
- 828 mL in 1 BOTTLE (42669-028-03)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "40941cb8-9e8f-44bb-857d-051ec271f213", "openfda": {"upc": ["0077443600050"], "unii": ["0F32U78V2Q"], "rxcui": ["413261"], "spl_set_id": ["fe624dde-c285-4a7f-965d-d878a38b2963"], "manufacturer_name": ["Davion, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "828 mL in 1 BOTTLE (42669-028-03)", "package_ndc": "42669-028-03", "marketing_start_date": "20250215"}], "brand_name": "Chloroxylenol 0.30 %", "product_id": "42669-028_40941cb8-9e8f-44bb-857d-051ec271f213", "dosage_form": "LIQUID", "product_ndc": "42669-028", "generic_name": "Chloroxylenol", "labeler_name": "Davion, Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Chloroxylenol 0.30 %", "active_ingredients": [{"name": "CHLOROXYLENOL", "strength": "3 mg/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250215", "listing_expiration_date": "20261231"}