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 - PURPOSE SECTION
OTC - ASK DOCTOR SECTION
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
OTC - DO NOT USE SECTION
OTC - STOP USE SECTION
OTC - WHEN USING SECTION
WARNINGS SECTION
DOSAGE & ADMINISTRATION SECTION
INDICATIONS & USAGE SECTION
INSTRUCTIONS FOR USE SECTION
OTHER SAFETY INFORMATION
INACTIVE INGREDIENT SECTION
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| c5cd4727-ac49-4409-82b1-5bd8006c3ec7 | Product name | 1 | 20171122 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 81309-009-01 | APPTI Face Sunscreen | 74 mL in 1 TUBE | LOTION | 74 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- APPTI Face Sunscreen
- Titanium Dioxide, Zinc Oxide, Octocrylene
- GREEN TEA LEAF
- POLYGLYCERYL-4 ISOSTEARATE
- HYALURONATE SODIUM
- ZINC OXIDE
- PHENOXYETHANOL
- 1,2-HEXANEDIOL
- WATER
- PANTHENOL
- TOCOPHEROL
- LEVOMENOL
- ETHYLHEXYLGLYCERIN
- TITANIUM DIOXIDE
- OCTOCRYLENE
- BUTYLENE GLYCOL
- CERAMIDE 3
- ASCORBIC ACID
- CERAMIDE 6 II, L-
- SILICA DIMETHYL SILYLATE
- CERAMIDE 1
- GLYCERIN
- HYDROXYACETOPHENONE
- CENTELLA ASIATICA TRITERPENOIDS
- REYNOUTRIA JAPONICA ROOT
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 81309-009 | 81309-009-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 228b6c84-90e8-eb5c-e063-6394a90a0c40 | 228b64a6-ba13-eb52-e063-6394a90a5320 | 2024-09-20 | Warnings | 228b6c84-90e8-eb5c-e063-6394a90a0c40 228b64a6-ba13-eb52-e063-6394a90a5320 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
