prime source antimicrobial foam so ap
Generic: chloroxylenol
Labeler: bunzlDrug Facts
Product Profile
Brand Name
prime source antimicrobial foam so ap
Generic Name
chloroxylenol
Labeler
bunzl
Dosage Form
LIQUID
Routes
Active Ingredients
chloroxylenol .003 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
66294-082
Product ID
66294-082_297cde7f-1eb7-4779-e063-6394a90a262e
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2026-12-31
Marketing Start
2007-12-15
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
66294082
Hyphenated Format
66294-082
Supplemental Identifiers
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
prime source antimicrobial foam so ap (source: ndc)
Generic Name
chloroxylenol (source: ndc)
Application Number
505G(a)(3) (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .003 mg/mL
Packaging
- 1200 mL in 1 PACKAGE (66294-082-40)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "297cde7f-1eb7-4779-e063-6394a90a262e", "openfda": {"unii": ["0F32U78V2Q"], "spl_set_id": ["294f2bee-1086-4f24-80c0-4be5885870ba"], "manufacturer_name": ["BUNZL"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1200 mL in 1 PACKAGE (66294-082-40)", "package_ndc": "66294-082-40", "marketing_start_date": "20071215"}], "brand_name": "PRIME SOURCE Antimicrobial Foam So ap", "product_id": "66294-082_297cde7f-1eb7-4779-e063-6394a90a262e", "dosage_form": "LIQUID", "product_ndc": "66294-082", "generic_name": "Chloroxylenol", "labeler_name": "BUNZL", "product_type": "HUMAN OTC DRUG", "brand_name_base": "PRIME SOURCE Antimicrobial Foam So ap", "active_ingredients": [{"name": "CHLOROXYLENOL", "strength": ".003 mg/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20071215", "listing_expiration_date": "20261231"}