Sunscreen

Manufacturer
SKIN KIDZ CC
Effective date
2018-06-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:56:03

Label at a glance#

ProductSunscreen SPF50
Active ingredientAvobenzone, HOMOSALATE, OCTISALATE, OXYBENZONE, OCTOCRYLENE
Label structure8 sections

Dosage and administration

● apply generously 15 minutes before sun exposure ● ensure complete coverage to the are above the lip, nose, and tops of ears ● reapply: - after 80 minutes of swimming or sweating – immediately after towel drying – at least every 2 hours.

Label contents#

Full prescribing information#

PURPOSE

OTC - PURPOSE SECTION

Sunscreen

Uses

● helps prevent sunburn

● if used as directed with other sun protection measures

  • decreases the risk of skin cancer and early skin aging caused by the sun 

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3%, Homosalate 11.7%,
Octisalate 4.5%, Oxybenzone 5.4%,
Octocrylene 4.5%

Directions 

INSTRUCTIONS FOR USE SECTION

● apply generously 15 minutes before sun exposure

● ensure complete coverage to the are above the lip, nose, and tops of ears

● reapply: - after 80 minutes of swimming or sweating – immediately after towel drying – at least every 2 hours.

WARNING AND Pracaution

WARNINGS AND PRECAUTIONS 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.

●If rash occurs, stop use and ask a doctor 

ASK DOCTOR SECTION

OTC - ASK DOCTOR SECTION

●If rash occurs, stop use and ask a doctor

KEEP OUT OF REACH OF CHILDREN SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • KEEP OUT OF REACH OF CHILDREN SECTION
  • If swallowed, get medical help or contact a Poison Control Center right away.

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

ingredients: water, propylene glycol,
polyurethane-34, cetyl alcohol, potassium cetyl
phosphate, glycerin, sorbitan mono stearate,
polysorbate 60, phenoxyethanol,
ethylhexylglycerin, potassium hydroxide,
dimethicone, tocopheryl acetate, acrylates/C10-
30 alkyl acrylate crosspolymer, arginine, sodium
ascorbyl phosphate, disodium EDTA

Product Label 

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

front imagefront imagedrug factsdrug facts

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
1681bc73-b05f-12c3-1075-382ae39f449cProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72376-001-012020-01-31C16284748780-19d75b9d1-02b2-f424-e053-dadaa90a57ceSun Skin SPF50 Sunscreen

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72376-001-01SunscreenSPF5051 g in 1 BOTTLELOTION511

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72376-001SUNSCREEN SPF50 (AVOBENZONE , HOMOSALATE , OCTISALATE , OXYBENZONE , OCTOCRYLENE) LOTION [SKIN KIDZ CC]1Legacy NDC, 1 package rows20180622_9819e603-8a87-408a-839d-e325493590aa.zip

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
72376-00172376-001-01

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
e897b9bb-5d62-469b-a29b-2ca6457455619819e603-8a87-408a-839d-e325493590aa2018-06-22WarningsExact identifier
spl id: e897b9bb-5d62-469b-a29b-2ca645745561
spl set id: 9819e603-8a87-408a-839d-e325493590aa

Reported adverse events (FAERS/openFDA)#

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