Dr. Nikko Sheer Sunscreen Broad Spectrum SPF 40

Manufacturer
Nikko Cosmetic Surgery Center | CIT Co.,Ltd.
Effective date
2019-12-11
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 23:53:05

Label at a glance#

ProductDr. Nikko Sheer Sunscreen Broad Spectrum SPF 40
Active ingredientOCTINOXATE, OCTISALATE, ENSULIZOLE
Label structure10 sections

Indications and uses

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.

Dosage and administration

Apply liberally 15 minutes before sun exposure. 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 or higher and other sun protection measures including: Limit time in the sun, especially from 10 a.m. - 2 p. m. Wear long-sleeve shirts, pants, hats, and sunglasses. Children under ...

Storage and handling

Protect this product from excessive heat and direct sun. Report serious adverse event to: Nikko Cosmetic Surgery Center 4707 Eigel St Suite 100 Houston, TX 77007

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Octinoxate - 7.0%
Octisalate - 4.5%
Ensulizole - 2%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE 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.

Warnings

WARNINGS SECTION

For external use only.

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin.

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

Stop use and ask a doctor if rash occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply liberally 15 minutes before sun exposure.
  • 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 or higher and other sun protection measures including:
    • Limit time in the sun, especially from 10 a.m. - 2 p. m.
    • Wear long-sleeve shirts, pants, hats, and sunglasses.
  • Children under 6 months: Ask a doctor.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water,Glycerin, Dipropylene Glycol, Diethylamino Hydroxybenzoyl Hexyl Benzoate, C12-15 Alkyl Benzoate, Cetearyl Olivate, Cetearyl Alcohol, Methyl Methacrylate Crosspolymer, Glyceryl Stearate, Sorbitan Olivate, Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine, Polyacrylate-13, Polysorbate 60, Dimethicone, Polyisobutene, Caprylyl Glycol, Sodium Hydroxide, Sorbitan Stearate, Ethylhexylglycerin, PEG-100 Stearate, Fragrance, Polysorbate 20, Sorbitan Isostearate, 1,2-Hexanediol, Disodium EDTA, Butylene Glycol, Prunus Amygdalus Dulcis (sweet Almond) Seed Extract, Pinus Sylvestris Bark Extract, Caprylic/Capric Triglyceride, Polyglyceryl-10 Diisostearate, Hydrogenated Lecithin, Phenoxyethanol, Pistacia Lentiscus (Mastic) Gum, Zingiber Officinale (Ginger) Root Extract, Tetrasodium EDTA, Hydrolyzed Hyaluronic Acid.

Other information

STORAGE AND HANDLING SECTION

  • Protect this product from excessive heat and direct sun.
  • Report serious adverse event to:
    Nikko Cosmetic Surgery Center
    4707 Eigel St Suite 100 Houston, TX 77007

Questions or comments?

OTC - QUESTIONS SECTION

832-906-2900 / M-T 9am -5pm F 9am-3pm

PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DR NIKKO
SKIN CARE

SHEER
SUNSCREEN
WITH SKIN MATRIX COMPLEX

SWEET ALMOND EXTRACT
PINE BARK EXTRACT

BROAD SPECTRUM

SPF 40

1.7 FL OZ (50mL)

dr nikkodr nikko

Products#

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

DailyMed product names page 1 of 1 · 39 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71651-00171651-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 37 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
996f7989-17d1-5b28-e053-2995a90af8b8faddc2e9-0ff9-4637-8cd8-6dc890a927062019-12-11WarningsExact identifier
spl id: 996f7989-17d1-5b28-e053-2995a90af8b8
spl set id: faddc2e9-0ff9-4637-8cd8-6dc890a92706

Reported adverse events (FAERS/openFDA)#

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