Package 87118-003-01

Brand: seavue dental desensitizer

Generic: potassium nitrate and sodium fluoride dentifrice
NDC Package

Package Facts

Identity

Package NDC 87118-003-01
Digits Only 8711800301
Product NDC 87118-003
Description

1 g in 1 BOX (87118-003-01)

Marketing

Marketing Status
Marketed Since 2025-10-08
Brand seavue dental desensitizer
Generic potassium nitrate and sodium fluoride dentifrice
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["DENTAL"], "spl_id": "3f47f399-1a15-5264-e063-6394a90aeb1c", "openfda": {"unii": ["RU45X2JN0Z", "8ZYQ1474W7"], "spl_set_id": ["3f47f399-1a14-5264-e063-6394a90aeb1c"], "manufacturer_name": ["Xiling (Zhenjiang) Medical Technology Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 g in 1 BOX (87118-003-01)", "package_ndc": "87118-003-01", "marketing_start_date": "20251008"}], "brand_name": "Seavue Dental Desensitizer", "product_id": "87118-003_3f47f399-1a15-5264-e063-6394a90aeb1c", "dosage_form": "GEL, DENTIFRICE", "product_ndc": "87118-003", "generic_name": "potassium nitrate and sodium fluoride dentifrice", "labeler_name": "Xiling (Zhenjiang) Medical Technology Co., Ltd.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Seavue Dental Desensitizer", "active_ingredients": [{"name": "POTASSIUM NITRATE", "strength": "26 mg/g"}, {"name": "SODIUM FLUORIDE", "strength": "1.36 mg/g"}], "application_number": "M022", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20251008", "listing_expiration_date": "20261231"}