Package 84878-200-02

Brand: sunsolve md correct and fade

Generic: zinc oxide
NDC Package

Package Facts

Identity

Package NDC 84878-200-02
Digits Only 8487820002
Product NDC 84878-200
Product ID 84878-200_4395a3a6-6fe6-e6b9-e063-6294a90ae938
Description

1 BOTTLE, PUMP in 1 CARTON (84878-200-02) / 48 mL in 1 BOTTLE, PUMP (84878-200-01)

Marketing

Marketing Status
Marketed Since 2024-11-06
Brand sunsolve md correct and fade
Generic zinc oxide
Sample Package No

Linked Drug Pages (1)

Sunsolve MD Correct and Fade ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "4395a3a6-6fe6-e6b9-e063-6294a90ae938", "openfda": {"upc": ["5061023120033"], "unii": ["SOI2LOH54Z"], "spl_set_id": ["26f3ad9f-f8ca-05d4-e063-6394a90ad5c4"], "manufacturer_name": ["Sunsolve MD Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PUMP in 1 CARTON (84878-200-02)  / 48 mL in 1 BOTTLE, PUMP (84878-200-01)", "package_ndc": "84878-200-02", "marketing_start_date": "20241106"}], "brand_name": "Sunsolve MD Correct and Fade", "product_id": "84878-200_4395a3a6-6fe6-e6b9-e063-6294a90ae938", "dosage_form": "LOTION", "product_ndc": "84878-200", "generic_name": "Zinc Oxide", "labeler_name": "Sunsolve MD Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sunsolve MD Correct and Fade", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "132 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20241106", "listing_expiration_date": "20261231"}