Package 37808-163-86

Brand: anticavity fluoride rinse

Generic: sodium fluoride
NDC Package

Package Facts

Identity

Package NDC 37808-163-86
Digits Only 3780816386
Product NDC 37808-163
Description

1000 mL in 1 BOTTLE, PLASTIC (37808-163-86)

Marketing

Marketing Status
Marketed Since 2010-09-29
Brand anticavity fluoride rinse
Generic sodium fluoride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4b93abb5-e1e0-0fb5-e063-6294a90a6683", "openfda": {"unii": ["8ZYQ1474W7"], "rxcui": ["1038904"], "spl_set_id": ["87327a36-a314-4daa-83b6-b4bd3e26bba2"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 mL in 1 BOTTLE, PLASTIC (37808-163-86)", "package_ndc": "37808-163-86", "marketing_start_date": "20100929"}], "brand_name": "Anticavity Fluoride Rinse", "product_id": "37808-163_4b93abb5-e1e0-0fb5-e063-6294a90a6683", "dosage_form": "MOUTHWASH", "product_ndc": "37808-163", "generic_name": "SODIUM FLUORIDE", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Anticavity Fluoride Rinse", "active_ingredients": [{"name": "SODIUM FLUORIDE", "strength": "1 mg/mL"}], "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20100929", "listing_expiration_date": "20271231"}