Package 35192-059-13

Brand: SONNE Face Body Sunscreen SPF 30

Generic: Sunscreen
NDC Package

Package Facts

Identity

Package NDC 35192-059-13
Digits Only 3519205913
Product NDC 35192-059
Description

118 g in 1 BOTTLE (35192-059-13)

Marketing

Marketing Status
Marketed Since 2025-05-05
Brand SONNE Face Body Sunscreen SPF 30
Generic Sunscreen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4628fc13-ad49-bdc9-e063-6394a90af640", "openfda": {"unii": ["SOI2LOH54Z"], "spl_set_id": ["355b266a-6623-76e7-e063-6394a90ab527"], "manufacturer_name": ["CA Botana International INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "118 g in 1 BOTTLE (35192-059-13)", "package_ndc": "35192-059-13", "marketing_start_date": "20250505"}], "brand_name": "SONNE Face Body Sunscreen SPF 30", "product_id": "35192-059_4628fc13-ad49-bdc9-e063-6394a90af640", "dosage_form": "EMULSION", "product_ndc": "35192-059", "generic_name": "Sunscreen", "labeler_name": "CA Botana International INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SONNE Face Body Sunscreen SPF 30", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "19.2 g/19.2g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250505", "listing_expiration_date": "20261231"}