OTC - ACTIVE INGREDIENT SECTION
Titanium Dioxide, Ethylhexyl Methoxycinnamate, Ethylhexyl Salicylate, Isoamyl p-Methoxycinnamate, Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine, Adenosine
Titanium Dioxide, Ethylhexyl Methoxycinnamate, Ethylhexyl Salicylate, Isoamyl p-Methoxycinnamate, Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine, Adenosine
Water, Butylene Glycol, etc.
Sun block, Skin whitening, Wrinkle reducer
keep out or reach of the children
Take the puff and press it into the cushion, then tap it all round your face to spread it evenly on your face.
Do not use on damaged or broken skin.
When using this product
• Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.
Stop use if following symptoms occur. (Continuing in usage may increase symptoms, ask doctor.)
1) If any red spots, swelling, itching, or skin irritation develops.
2) If direct sunlight causes irritation
Keep out of reach of children
• Do not swallow. In case of accidental ingestion, get medical help or contact a Poison Control
Center right away.
Store at room temperature
•
Close lid after use – possibility of contamination may exists if displaced contents are replaced back to container.
for external use only
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 71673-0007-1 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-b91a-f424-e053-dadaa90a57ce | 577a5cc2-5905-7777-e053-2a91aa0a2ba1 |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 71673-0007-1 | DPC PINK AURA CUSHION NO.21 | 15 g in 1 CONTAINER | LIQUID | 15 | 2 |
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 71673-0007 | DPC PINK AURA CUSHION NO.21 (TITANIUM DIOXIDE, ETHYLHEXYL METHOXYCINNAMATE, ETHYLHEXYL SALICYLATE, ISOAMYL P-METHOXYCINNAMATE, NIACINAMIDE, BIS-ETHYLHEXYLOXYPHENOL METHOXYPHENYL TRIAZINE, ADENOSINE) LIQUID [MSCO] | 2 | Legacy NDC, 1 package rows | 20170824_577a5cc2-5905-7777-e053-2a91aa0a2ba1.zip |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 71673-0007 | 71673-0007-1 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WATER | 059QF0KO0R | IACT |
| OCTINOXATE | 4Y5P7MUD51 | ACTIB |
| AMILOXATE | 376KTP06K8 | ACTIB |
| OCTISALATE | 4X49Y0596W | ACTIB |
| BEMOTRIZINOL | PWZ1720CBH | ACTIB |
| TITANIUM DIOXIDE | 15FIX9V2JP | ACTIB |
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 |
|---|---|---|---|---|---|---|
| 577aea49-609b-3ede-e053-2991aa0a0283 | 577a5cc2-5905-7777-e053-2a91aa0a2ba1 | 2017-08-24 | Warnings | 577aea49-609b-3ede-e053-2991aa0a0283 577a5cc2-5905-7777-e053-2a91aa0a2ba1 |
Adverse event summaries are temporarily unavailable. Other product information remains available.