Package 84126-616-38

Brand: crest 3d white brilliance pro ultra white

Generic: sodium monofluorophosphate
NDC Package

Package Facts

Identity

Package NDC 84126-616-38
Digits Only 8412661638
Product NDC 84126-616
Description

1 TUBE in 1 CARTON (84126-616-38) / 107 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2025-06-01
Brand crest 3d white brilliance pro ultra white
Generic sodium monofluorophosphate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "47e53ade-9e73-6d74-e063-6294a90a8493", "openfda": {"unii": ["C810JCZ56Q"], "rxcui": ["1038995"], "spl_set_id": ["338acdf2-548c-0614-e063-6294a90af635"], "manufacturer_name": ["The Procter & Gamble Manufacturing Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (84126-616-38)  / 107 g in 1 TUBE", "package_ndc": "84126-616-38", "marketing_start_date": "20250601"}], "brand_name": "Crest 3D White Brilliance Pro Ultra White", "product_id": "84126-616_47e53ade-9e73-6d74-e063-6294a90a8493", "dosage_form": "PASTE, DENTIFRICE", "product_ndc": "84126-616", "generic_name": "Sodium monofluorophosphate", "labeler_name": "The Procter & Gamble Manufacturing Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Crest 3D White", "brand_name_suffix": "Brilliance Pro Ultra White", "active_ingredients": [{"name": "SODIUM MONOFLUOROPHOSPHATE", "strength": "1.7 mg/g"}], "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250601", "listing_expiration_date": "20271231"}