SHINEBLOCK

Manufacturer
USRX LLC | Gordon Laboratories, Inc.
Effective date
2022-10-13
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:51:42

Label at a glance#

ProductSHINEBLOCK
Active ingredientZINC OXIDE
Label structure8 sections

Dosage and administration

For sunscreen use: Apply liberally and evenly 15 minutes before sun exposure Reapply at least every 2 hours Use a water resistant sunscreen if swimming or seating 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 value of 15 or higher and other sun protection measures including: Limit...

Label contents#

Full prescribing information#

Active Ingredients:

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 11.6%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Use(s):

INDICATIONS & USAGE SECTION

Helps prevent sunburn.

If used as directed with other sun protection measures (see directions), decreases the risk of skin canger and early skin aging caused by the sun.

Warnings:

WARNINGS SECTION

For External use only.

Do not use

OTC - DO NOT USE SECTION

on damaged or broken skin.

When using this product,

OTC - WHEN USING SECTION

keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor

OTC - STOP USE SECTION

if rash occurs.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions:

DOSAGE & ADMINISTRATION SECTION

For sunscreen use:

  • Apply liberally and evenly 15 minutes before sun exposure
  • Reapply at least every 2 hours
  • Use a water resistant sunscreen if swimming or seating

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 value of 15 or higher and other sun protection measures including:

  • Limit time in the sun, especially from 10 a.m. to 2 p.m.
  • Wear long-sleeved shirts, pants, hats and sunglasses
  • Children under 6 months: ask a doctor

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Water (Aqua), Butyloctyl Salicylate, Caprylic/Capric Triglyceride, Undecylcrylene Dimethicone, Glycerin, Silica, Cetearyl Olivate, Polyester-8, Polyglyceryl-3 Beeswax, Tapioca Starch, Carthamus Tinctorius (Safflower) Oleosomes, Sorbitan Olivate, Propanediol, Polyhydroxystearic Acid, Potassium Cetyl Phosphate, Caprylyl Glycol, Xanthan Gum, Bisabolol, Caprylhydroxamic Acid, Cinnamomum Camphora (Camphor) Bark Oil, Mentha Piperita (Peppermint) Oil, Sodium Gluconate, Carthamus Tinctorius (Safflower) Seedcake Extract.

Other Information:

OTHER SAFETY INFORMATION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

112233

FDA-Initiated Inactive NDC Indexing#

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70809-191170809-1911-1, 70809-1911-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 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
236fee3b-15ef-95f0-e063-6394a90a0b1cc790a30b-0262-3cda-e053-2995a90a0a0f2024-10-01WarningsExact identifier
spl set id: c790a30b-0262-3cda-e053-2995a90a0a0f

Reported adverse events (FAERS/openFDA)#

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