Storage and handling
Storage and Handling: - To keep the freshness, please close the lid after the use - Do not store this product in a place of high or low temperature - Do not expose it to the direct sunlight
QT SUN BLOCK
- Manufacturer
- Cleansia Co Ltd
- Effective date
- 2010-01-21
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 22:23:18
Label at a glance#
ProductQT SUN BLOCK
Active ingredientOCTINOXATE, TITANIUM DIOXIDE, ENZACAMENE
Label structure8 sections
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active Ingredients:
Ethylhexyl Methoxycinnamate, Titanium Dioxide, 4-Methylbenzylidene Camphor, Methylene Bis-Benzotriazolyl Tetramethylbutylphenol, Benzophenone-3
Ethylhexyl Methoxycinnamate, Titanium Dioxide, 4-Methylbenzylidene Camphor, Methylene Bis-Benzotriazolyl Tetramethylbutylphenol, Benzophenone-3
INACTIVE INGREDIENT SECTION
Inactive Ingredients:
Water, Cyclopentasiloxane, Disteardimonium Hectorite, Dimethiconol, Tocopheryl Acetate, PEG-10 Dimethicone, Cetyl PEG/PPG-10/1 Dimethicone, Sorbitan Sesquioleate, Glyceryl Behenate/Eicosadioate, Cetyl Ethylhexanoate, Cyclohexasiloxane, Propylene Glycol, Dipropylene Glycol, Allantoin, Aluminum Hydroxide, Stearic Acid, Xanthan Gum, Methylparaben, Sodium Chloride, Butylparaben, Imidazolidinyl Urea, Fragrance, Ethylparaben, Oryza Sativa (Rice) bran Oil, Oryza Sativa (Rice) Bran Extract
Water, Cyclopentasiloxane, Disteardimonium Hectorite, Dimethiconol, Tocopheryl Acetate, PEG-10 Dimethicone, Cetyl PEG/PPG-10/1 Dimethicone, Sorbitan Sesquioleate, Glyceryl Behenate/Eicosadioate, Cetyl Ethylhexanoate, Cyclohexasiloxane, Propylene Glycol, Dipropylene Glycol, Allantoin, Aluminum Hydroxide, Stearic Acid, Xanthan Gum, Methylparaben, Sodium Chloride, Butylparaben, Imidazolidinyl Urea, Fragrance, Ethylparaben, Oryza Sativa (Rice) bran Oil, Oryza Sativa (Rice) Bran Extract
OTC - WHEN USING SECTION
Directions:
When you use or do leisure, apply reasonable amount on your body exposed to UV including face, neck, arms and legs at your finishing step of basic makeup. Take more frequent reapplication for long time outdoor activities
When you use or do leisure, apply reasonable amount on your body exposed to UV including face, neck, arms and legs at your finishing step of basic makeup. Take more frequent reapplication for long time outdoor activities
OTC - DO NOT USE SECTION
Notice for Use:
1. Discontinue if the following symptom appears and consult with dermatologist for the continuous problem of use
a) Discontinue use if redness, rash, irritation or tingling appears
b) Discontinue if the above symptom appears by a direct sunlight on the applied part
2. Avoid the part for a cut, eczema or dermatitis
1. Discontinue if the following symptom appears and consult with dermatologist for the continuous problem of use
a) Discontinue use if redness, rash, irritation or tingling appears
b) Discontinue if the above symptom appears by a direct sunlight on the applied part
2. Avoid the part for a cut, eczema or dermatitis
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep this and all drugs out of reach of children
PRECAUTIONS SECTION
Caution:
- Be careful it may be slippery when contact with the product
- Be careful not to make contact with clothes
- Be careful not to give a shock since the container may be broken and get injured
- Be careful it may be slippery when contact with the product
- Be careful not to make contact with clothes
- Be careful not to give a shock since the container may be broken and get injured
STORAGE AND HANDLING SECTION
Storage and Handling:
- To keep the freshness, please close the lid after the use
- Do not store this product in a place of high or low temperature
- Do not expose it to the direct sunlight
- To keep the freshness, please close the lid after the use
- Do not store this product in a place of high or low temperature
- Do not expose it to the direct sunlight
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 45167-516-16 | 2019-10-21 | C162847 | 48780-1 | 956f9ecf-d4c1-621f-e053-dbdaa90a74ad | 80e07a95-6249-49b2-8610-c430b9fcd5b4 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 45167-516-16 | QT SUN BLOCK | 100 g in 1 TUBE | CREAM | 100 | 1 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| ENZACAMENE | ACTIVE INGREDIENT | 8I3XWY40L9 | 1 | |
| OCTINOXATE | ACTIVE INGREDIENT | 4Y5P7MUD51 | 1 | |
| TITANIUM DIOXIDE | ACTIVE INGREDIENT | 15FIX9V2JP | 1 | |
| ENZACAMENE | ACTIVE MOIETY | 8I3XWY40L9 | 1 | |
| OCTINOXATE | ACTIVE MOIETY | 4Y5P7MUD51 | 1 | |
| TITANIUM DIOXIDE | ACTIVE MOIETY | 15FIX9V2JP | 1 |
Products#
Every source-derived product name is available through these pages.
- QT SUN BLOCK
- OCTINOXATE, TITANIUM DIOXIDE, ENZACAMENE
- OCTINOXATE
- TITANIUM DIOXIDE
- ENZACAMENE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 45167-516 | 45167-516-16 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| OCTINOXATE | 4Y5P7MUD51 | ACTIB |
| TITANIUM DIOXIDE | 15FIX9V2JP | ACTIB |
| ENZACAMENE | 8I3XWY40L9 | ACTIB |
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 |
|---|---|---|---|---|---|---|
| b5ab35c8-9590-4ff4-9c71-3d19867ec713 | 80e07a95-6249-49b2-8610-c430b9fcd5b4 | 2010-01-21 | b5ab35c8-9590-4ff4-9c71-3d19867ec713 80e07a95-6249-49b2-8610-c430b9fcd5b4 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.