Package 69949-052-01

Brand: 5-in-1 tinted face sunscreen - light

Generic: zinc oxide
NDC Package

Package Facts

Identity

Package NDC 69949-052-01
Digits Only 6994905201
Product NDC 69949-052
Description

56.7 g in 1 TUBE (69949-052-01)

Marketing

Marketing Status
Marketed Since 2013-07-01
Brand 5-in-1 tinted face sunscreen - light
Generic zinc oxide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "2c5a7500-d9ee-4d1b-b79d-c7adb8e70faf", "openfda": {"unii": ["SOI2LOH54Z"], "spl_set_id": ["c0892856-cd12-4c1f-8420-866dbd0f8907"], "manufacturer_name": ["Synchronicity Spa, Inc. DBA Suntegrity"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "56.7 g in 1 TUBE (69949-052-01)", "package_ndc": "69949-052-01", "marketing_start_date": "20130701"}], "brand_name": "5-IN-1 TINTED FACE SUNSCREEN - LIGHT", "product_id": "69949-052_2c5a7500-d9ee-4d1b-b79d-c7adb8e70faf", "dosage_form": "CREAM", "product_ndc": "69949-052", "generic_name": "Zinc Oxide", "labeler_name": "Synchronicity Spa, Inc. DBA Suntegrity", "product_type": "HUMAN OTC DRUG", "brand_name_base": "5-IN-1 TINTED FACE SUNSCREEN - LIGHT", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "200 mg/g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20130701", "listing_expiration_date": "20261231"}