Package 81136-001-01

Brand: spf 30 daily sunscreen

Generic: zinc oxide
NDC Package

Package Facts

Identity

Package NDC 81136-001-01
Digits Only 8113600101
Product NDC 81136-001
Product ID 81136-001_1250ff1a-90a4-9d47-e063-6394a90ad3ae
Description

1 TUBE in 1 CARTON (81136-001-01) / 50 mL in 1 TUBE

Marketing

Marketing Status
Marketed Since 2021-04-19
Brand spf 30 daily sunscreen
Generic zinc oxide
Sample Package No

Linked Drug Pages (1)

SPF 30 Daily Sunscreen ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "1250ff1a-90a4-9d47-e063-6394a90ad3ae", "openfda": {"upc": ["5060422298701"], "unii": ["SOI2LOH54Z"], "spl_set_id": ["c0541f32-f072-3630-e053-2a95a90a12d6"], "manufacturer_name": ["Brand Evangelists for Beauty Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (81136-001-01)  / 50 mL in 1 TUBE", "package_ndc": "81136-001-01", "marketing_start_date": "20210419"}], "brand_name": "SPF 30 Daily Sunscreen", "product_id": "81136-001_1250ff1a-90a4-9d47-e063-6394a90ad3ae", "dosage_form": "CREAM", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "81136-001", "generic_name": "ZINC OXIDE", "labeler_name": "Brand Evangelists for Beauty Ltd.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SPF 30 Daily Sunscreen", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "220 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210419", "listing_expiration_date": "20261231"}