Package 50555-210-02

Brand: foamgle foam mouthwash super mint

Generic: allantoin
NDC Package

Package Facts

Identity

Package NDC 50555-210-02
Digits Only 5055521002
Product NDC 50555-210
Product ID 50555-210_352342bf-e2de-3a2c-e063-6294a90a200e
Description

1 BOTTLE in 1 CARTON (50555-210-02) / 50 mL in 1 BOTTLE (50555-210-01)

Marketing

Marketing Status
Marketed Since 2025-05-01
Brand foamgle foam mouthwash super mint
Generic allantoin
Sample Package No

Linked Drug Pages (1)

Foamgle Foam Mouthwash Super Mint ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "352342bf-e2de-3a2c-e063-6294a90a200e", "openfda": {"unii": ["344S277G0Z"], "spl_set_id": ["352342bf-e2dd-3a2c-e063-6294a90a200e"], "manufacturer_name": ["KMPHARMACEUTICAL CO.,LTD"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (50555-210-02)  / 50 mL in 1 BOTTLE (50555-210-01)", "package_ndc": "50555-210-02", "marketing_start_date": "20250501"}], "brand_name": "Foamgle Foam Mouthwash Super Mint", "product_id": "50555-210_352342bf-e2de-3a2c-e063-6294a90a200e", "dosage_form": "LIQUID", "product_ndc": "50555-210", "generic_name": "Allantoin", "labeler_name": "KMPHARMACEUTICAL CO.,LTD", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Foamgle Foam Mouthwash Super Mint", "active_ingredients": [{"name": "ALLANTOIN", "strength": ".05 g/100mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20250501", "listing_expiration_date": "20261231"}