Package 54108-0418-1

Brand: derma e sun defense spf 30

Generic: zinc oxide and titanium dioxide
NDC Package

Package Facts

Identity

Package NDC 54108-0418-1
Digits Only 5410804181
Product NDC 54108-0418
Product ID 54108-0418_61d20f28-5db0-4155-84f2-10302b84002e
Description

1 TUBE in 1 BOX (54108-0418-1) / 113 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2022-12-30
Brand derma e sun defense spf 30
Generic zinc oxide and titanium dioxide
Sample Package No

Linked Drug Pages (1)

Derma E Sun Defense SPF 30 ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "61d20f28-5db0-4155-84f2-10302b84002e", "openfda": {"unii": ["15FIX9V2JP", "SOI2LOH54Z"], "spl_set_id": ["395b73a4-dae7-49da-9dab-ab622117c8c0"], "manufacturer_name": ["derma e"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 BOX (54108-0418-1)  / 113 g in 1 TUBE", "package_ndc": "54108-0418-1", "marketing_start_date": "20221230"}], "brand_name": "Derma E Sun Defense SPF 30", "product_id": "54108-0418_61d20f28-5db0-4155-84f2-10302b84002e", "dosage_form": "LOTION", "product_ndc": "54108-0418", "generic_name": "Zinc Oxide and Titanium Dioxide", "labeler_name": "derma e", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Derma E Sun Defense", "brand_name_suffix": "SPF 30", "active_ingredients": [{"name": "TITANIUM DIOXIDE", "strength": "26.4 mg/g"}, {"name": "ZINC OXIDE", "strength": "195 mg/g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20221230", "listing_expiration_date": "20261231"}