ACWELL SOLAR DEFENSE LICORICE C BLEMISH Sunstick

Manufacturer
BNHCOSMETICS CO., LTD. | Cosmax, Inc.
Effective date
2022-10-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:51:51

Label at a glance#

ProductACWELL SOLAR DEFENSE LICORICE C BLEMISH Sunstick
Active ingredientTITANIUM DIOXIDE, ZINC OXIDE
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 22.63%

Titanium Dioxide 4.46%

OTC - PURPOSE SECTION

Sunscreen

DOSAGE & ADMINISTRATION SECTION

- Apply liberally 15 minutes before sun exposure. Reapply at least every two 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 of 15 of higher and other sun protection measures including: 1) Limited time in the sun, especially from 10 am to 2 pm. 2) Wear long-sleeve shirts, pants, hats, and sunglasses
- Ask a doctor to use for children under 6 months

INDICATIONS & USAGE SECTION

Helps prevent sunburn

WARNINGS SECTION

For external use only

Do not use on damaged or broken skin

When using this product, keep out of eyes. Rinse with water to remove.

Stop using and ask a doctor if rash occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of the children. If product is swallowed, get medical help or contact a poison control center right away.

INACTIVE INGREDIENT SECTION

Diphenylsiloxy Phenyl Trimethicone, Coco-Caprylate/Caprate, Butyloctyl Salicylate, Polyphenylsilsesquioxane, Mica (CI 77019), Octyldodecanol, Synthetic Wax, Diglyceryl Sebacate/Isopalmitate, Paraffin, Tridecyl Trimellitate, Polyhydroxystearic Acid, Silica, Caprylic/Capric Triglyceride, Methyl Methacrylate Crosspolymer, Triethoxycaprylylsilane, Glycyrrhiza Glabra (Licorice) Root Extract, Spirulina Maxima Extract, Poterium Officinale Root Extract, Veronica Officinalis Extract, Euphorbia Cerifera (Candelilla) Wax, Polyglyceryl-2 Triisostearate, Microcrystalline Wax, Lecithin, Ethylhexyl Palmitate, Isopropyl Myristate, Isostearic Acid, Vinyl Dimethicone/Methicone Silsesquioxane Crosspolymer, Polyglyceryl-3 Polyricinoleate, Caprylyl Glycol, Glyceryl Caprylate, Diisostearyl Malate, Water, Ascorbic Acid, Ascorbic Acid Polypeptide, Sucrose, Butylene Glycol, 1,2-Hexanediol, Iron Oxides (CI 77492), Iron Oxides (CI 77491), Iron Oxides (CI 77499)

OTHER SAFETY INFORMATION

Protect the product in the container from excessive heat and direct sun

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71597-01271597-012-01, 71597-012-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 39 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
face1079-4376-45aa-e053-6394a90ad1795e24b0cb-9f47-43d3-950d-3df5f54f9f202023-05-03WarningsExact identifier
spl set id: 5e24b0cb-9f47-43d3-950d-3df5f54f9f20

Reported adverse events (FAERS/openFDA)#

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