OTC - ACTIVE INGREDIENT SECTION
OCTOCRYLENE 2%
VUINT TINTED SUNSCREEN
- Manufacturer
- Hainan Shengtaizhuo International Information Development Co., LTD
- Effective date
- 2024-09-29
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 20:52:52
Label at a glance#
ProductVUINT TINTED SUNSCREEN
Active ingredientOCTOCRYLENE
Label structure8 sections
Label contents#
Full prescribing information#
WARNINGS SECTION
For external use only.
Do not use on damaged or broken skin. Stop use and ask a doctor if rash occurs.
When using this product keep out of eyes. Rinse with water to remove.
Keep out of reach of children. If swallowed, get medical help or contact a poison control center right away.
OTC - PURPOSE SECTION
Sunscreen
OTC - WHEN USING SECTION
Helps prevent sunburn - If used as directed with other sun protection measures (see DIRECTIONS), decreases the risk of skin cancer and early skin aging caused by the sun.
INDICATIONS & USAGE SECTION
Apply liberally 15 minutes before sun exposure • Reapply: • after 40 minutes of swimming or sweating • immediately after towel drying • at least every 2 hours
Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging.To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: limit time in the sun, especially from 10 a.m.-2 p.m. • wear long-sleeved shirts, pants, hats, and sunglasses • children under 6 months of age: ask a doctor
INACTIVE INGREDIENT SECTION
WATER、CYCLOPENTASILOXAN、AMINOMETHYL PROPANEDIOL、WATER、CI 77891、ALUMINA、LAUROYL LYSINE、ETHYLHEXYL METHOXYCINNAMATE、ETHYLHEXYL SALICYLATE、ISONONYL ISONONANOATE、LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE、PHENYLBENZIMIDAZOLE SULFONIC ACID、IETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE、DIISOSTEARYL MALATE、CETYL PEG/PPG-10/1 DIMETHICONE、TRIMETHYLSILOXYSILICATE、SODIUM CHLORIDE、POLYETHYLENE、TRIETHOXYCAPRYLYLSILANE、QUATERNIUM-18 BENTONITE、SODIUM HYDROXIDE、PHENOXYETHANOL、CI 77491、DIPOTASSIUM GLYCYRRHIZATE、GLYCYRRHIZA GLABRA EXTRACT、CI 77499、SODIUM HYALURONATE、FRAGRANCE
DOSAGE & ADMINISTRATION SECTION
Helps prevent sunburn. - If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
TINTED SUNSCREEN
VUINT
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 84556-929-01 | 2025-09-27 | C162847 | 48780-1 | 3b156c62-3226-fb37-e063-e6dba90a4e07 | 233f3ccf-df2c-7191-e063-6394a90a0ec2 |
| 84556-929-01 | 2025-07-29 | C162847 | 48780-1 | 3b156c62-3226-fb37-e063-e6dba90a4e07 | 233f3ccf-df2c-7191-e063-6394a90a0ec2 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- VUINT TINTED SUNSCREEN
- OCTOCRKYENE
- LAUROYL LYSINE
- DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE
- METHYLPROPANEDIOL
- DIISOSTEARYL MALATE
- TRIETHOXYCAPRYLYLSILANE
- PHENOXYETHANOL
- ISONONYL ISONONANOATE
- LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE
- SODIUM CHLORIDE
- WATER
- SODIUM HYDROXIDE
- OCTOCRYLENE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 84556-929 | 84556-929-01 |
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 |
|---|---|---|---|---|---|---|
| 3fca7931-0690-5de2-e063-6394a90abac9 | 233f3ccf-df2c-7191-e063-6394a90a0ec2 | 2025-09-27 | Warnings | 233f3ccf-df2c-7191-e063-6394a90a0ec2 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.