UV Defense Sun Block Tissues (BROAD SPECTRUM, SPF30)

Manufacturer
C&TECH CORPORATION
Effective date
2019-12-06
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:55:25

Label at a glance#

ProductUV Defense Sun Block Tissues (BROAD SPECTRUM, SPF30)
Active ingredientOCTOCRYLENE, AVOBENZONE, OCTISALATE, HOMOSALATE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

octocrylene, homosalate, ethylhexyl salicylate (OCTISALATE), butyl methoxydibenzoylmethane (AVOBENZONE)

INACTIVE INGREDIENT SECTION

methylpropanediol, alcohol denat., undecane, tridecane, glycine, serine, etc.

OTC - PURPOSE SECTION

sun protect

WARNINGS SECTION

1. If the following symptoms occur after product use, stop using the product immediately and consult a dermatologist (continuous use can exacerbate the symptoms).
1) Occurrence of red spots, swelling, itchiness, and other skin irritation
2) If the symptoms above occur after the application area is exposed to direct sunlight

2. Do not use on open wounds, eczema, and other skin irritations
3. Precaution for Storage and Handling
1) Close the lid after use
2) Keep out of reach of infants and children
3) Do not to store in a place with high/low temperature and exposed to direct sunlight

4. Use as avoiding eye areas.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

INDICATIONS & USAGE SECTION

1. Rub the surface of the pouch evenly before use to avoid the content from settling down.

2. Lift the front seal and pull out one sheet. Spread evenly over face, neck and arm which are most likely to get sun damage.

3. Make sure to reseal the pouch after each use.

DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71621-001271621-0012-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
99037a7d-0f65-74ea-e053-2a95a90a36216856a354-e851-10cc-e053-2a91aa0a5e702019-12-06WarningsExact identifier
spl id: 99037a7d-0f65-74ea-e053-2a95a90a3621
spl set id: 6856a354-e851-10cc-e053-2a91aa0a5e70

Reported adverse events (FAERS/openFDA)#

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