SPF50 Sunscreen

Manufacturer: KINGKEY MBC LIFE TECHNOLOGY GROUP CO., LTD
Effective date: 2025-10-07
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: full-release
Hydrated at: 2026-06-01 01:38:38

Label at a glance#

ProductSPF50 Sunscreen

Active ingredientTITANIUM DIOXIDE, ZINC OXIDE, HOMOSALATE, OCTOCRYLENE, OXYBENZONE

Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

80ml in 1 TUBE NDC: 73928-010-01

80ml label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73928-010-01	SPF50 Sunscreen	80 mL in 1 TUBE	CREAM	80		4

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 8 matching rows.

SPF50 Sunscreen
Sunscreen
WATER
TITANIUM DIOXIDE
ZINC OXIDE
HOMOSALATE
OCTOCRYLENE
OXYBENZONE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
73928-010	73928-010-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
TITANIUM DIOXIDE	15FIX9V2JP	ACTIB
ZINC OXIDE	SOI2LOH54Z	ACTIB
HOMOSALATE	V06SV4M95S	ACTIB
OCTOCRYLENE	5A68WGF6WM	ACTIB
OXYBENZONE	95OOS7VE0Y	ACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
3	2024-11-18	full-release	2026-06-01 00:37:51

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
SPF50 Sunscreen	SUNSCREEN	KINGKEY MBC LIFE TECHNOLOGY GROUP CO., LTD	b3cde609-7d62-2ac7-e053-2a95a90a26b3	2025-10-07		Exact identifier ndc (package): 73928-010-01 ndc (product): 73928-010 ndc11 (package): 73928001001 spl id: 40979dfb-f669-17bd-e063-6394a90ac717 spl set id: b3cde609-7d62-2ac7-e053-2a95a90a26b3

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.