alcohol free
Generic: cetylpyridinium cloride
Labeler: h e bDrug Facts
Product Profile
Brand Name
alcohol free
Generic Name
cetylpyridinium cloride
Labeler
h e b
Dosage Form
MOUTHWASH
Routes
Active Ingredients
cetylpyridinium chloride .7 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
37808-299
Product ID
37808-299_4b93d5b6-9abe-55e7-e063-6294a90a128d
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2027-12-31
Marketing Start
2009-04-16
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
37808299
Hyphenated Format
37808-299
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
alcohol free (source: ndc)
Generic Name
cetylpyridinium cloride (source: ndc)
Application Number
505G(a)(3) (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .7 mg/mL
Packaging
- 1000 mL in 1 BOTTLE, PLASTIC (37808-299-86)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4b93d5b6-9abe-55e7-e063-6294a90a128d", "openfda": {"unii": ["D9OM4SK49P"], "rxcui": ["1100924"], "spl_set_id": ["9787c416-e2c6-49f9-817f-ef1df3857583"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 mL in 1 BOTTLE, PLASTIC (37808-299-86)", "package_ndc": "37808-299-86", "marketing_start_date": "20090416"}], "brand_name": "Alcohol Free", "product_id": "37808-299_4b93d5b6-9abe-55e7-e063-6294a90a128d", "dosage_form": "MOUTHWASH", "product_ndc": "37808-299", "generic_name": "Cetylpyridinium cloride", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Alcohol Free", "active_ingredients": [{"name": "CETYLPYRIDINIUM CHLORIDE", "strength": ".7 mg/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20090416", "listing_expiration_date": "20271231"}