APPTI Face Sunscreen

Manufacturer
LYW BIOTECH CO LIMITED GUANGZHOU
Effective date
2024-09-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:19:52

Label at a glance#

ProductAPPTI Face Sunscreen
Active ingredientZINC OXIDE, TITANIUM DIOXIDE, OCTOCRYLENE
Label structure14 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

22

OTC - PURPOSE SECTION

33

OTC - ASK DOCTOR SECTION

44

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

55

OTC - DO NOT USE SECTION

66

OTC - STOP USE SECTION

77

OTC - WHEN USING SECTION

88

WARNINGS SECTION

99

DOSAGE & ADMINISTRATION SECTION

1010

INDICATIONS & USAGE SECTION

1414

INSTRUCTIONS FOR USE SECTION

1111

OTHER SAFETY INFORMATION

1212

INACTIVE INGREDIENT SECTION

1313

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81309-009-01APPTI Face Sunscreen74 mL in 1 TUBELOTION741

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81309-009APPTI FACE SUNSCREEN (TITANIUM DIOXIDE, ZINC OXIDE, OCTOCRYLENE) LOTION [LYW BIOTECH CO LIMITED GUANGZHOU]11 package rows20240921_228b64a6-ba13-eb52-e063-6394a90a5320.zip

Products#

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

DailyMed product names page 1 of 1 · 25 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81309-00981309-009-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 23 matching rows.

Source Document#

Source XML

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
228b6c84-90e8-eb5c-e063-6394a90a0c40228b64a6-ba13-eb52-e063-6394a90a53202024-09-20WarningsExact identifier
spl id: 228b6c84-90e8-eb5c-e063-6394a90a0c40
spl set id: 228b64a6-ba13-eb52-e063-6394a90a5320

Reported adverse events (FAERS/openFDA)#

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