primory antimicrobial foam
Generic: chloroxylenol
Labeler: gojo industries, inc.Drug Facts
Product Profile
Brand Name
primory antimicrobial foam
Generic Name
chloroxylenol
Labeler
gojo industries, inc.
Dosage Form
LIQUID
Routes
Active Ingredients
chloroxylenol .003 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
21749-555
Product ID
21749-555_27d4814b-9337-65eb-e063-6394a90add35
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2026-12-31
Marketing Start
2004-09-09
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
21749555
Hyphenated Format
21749-555
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
primory antimicrobial foam (source: ndc)
Generic Name
chloroxylenol (source: ndc)
Application Number
505G(a)(3) (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .003 mg/mL
Packaging
- 1250 mL in 1 PACKAGE (21749-555-90)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "27d4814b-9337-65eb-e063-6394a90add35", "openfda": {"unii": ["0F32U78V2Q"], "spl_set_id": ["18549702-f95f-447f-a551-4c2156f0667d"], "manufacturer_name": ["GOJO Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1250 mL in 1 PACKAGE (21749-555-90)", "package_ndc": "21749-555-90", "marketing_start_date": "20040909"}], "brand_name": "PRIMORY Antimicrobial Foam", "product_id": "21749-555_27d4814b-9337-65eb-e063-6394a90add35", "dosage_form": "LIQUID", "product_ndc": "21749-555", "generic_name": "Chloroxylenol", "labeler_name": "GOJO Industries, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "PRIMORY Antimicrobial Foam", "active_ingredients": [{"name": "CHLOROXYLENOL", "strength": ".003 mg/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20040909", "listing_expiration_date": "20261231"}