zep professional mild ab
Generic: benzalkonium chloride
Labeler: zep inc.Drug Facts
Product Profile
Brand Name
zep professional mild ab
Generic Name
benzalkonium chloride
Labeler
zep inc.
Dosage Form
LIQUID
Routes
Active Ingredients
benzalkonium chloride .13 g/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
66949-130
Product ID
66949-130_46de7e91-c4ca-2456-e063-6294a90a5a97
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2026-12-31
Marketing Start
2016-03-10
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
66949130
Hyphenated Format
66949-130
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
zep professional mild ab (source: ndc)
Generic Name
benzalkonium chloride (source: ndc)
Application Number
505G(a)(3) (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .13 g/100mL
Packaging
- 6000 mL in 1 CASE (66949-130-06)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "46de7e91-c4ca-2456-e063-6294a90a5a97", "openfda": {"unii": ["F5UM2KM3W7"], "rxcui": ["1046593"], "spl_set_id": ["b43b2607-a546-5109-e053-2a95a90a889e"], "manufacturer_name": ["Zep Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6000 mL in 1 CASE (66949-130-06)", "package_ndc": "66949-130-06", "marketing_start_date": "20160310"}], "brand_name": "Zep Professional Mild AB", "product_id": "66949-130_46de7e91-c4ca-2456-e063-6294a90a5a97", "dosage_form": "LIQUID", "product_ndc": "66949-130", "generic_name": "Benzalkonium Chloride", "labeler_name": "Zep Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Zep Professional Mild AB", "active_ingredients": [{"name": "BENZALKONIUM CHLORIDE", "strength": ".13 g/100mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20160310", "listing_expiration_date": "20261231"}