FDA.reportPublic FDA data

CVS Pharmacy

Manufacturer
CVS Pharmacy
Effective date
2022-05-16
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 22:01:14

Label at a glance#

ProductCVS Pharmacy SPF 50 Beach Guard Sun
Active ingredientOXYBENZONE, OCTOCRYLENE, HOMOSALATE, AVOBENZONE, OCTISALATE
Label structure12 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 • reapply: • after 80 minutes of swimming or sweating • immediately after towel drying • at least every 2 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 value of 15 or higher and other sun protection measures including: • lim...

Storage and handling

• protect the product in this container from excessive heat and direct sun • may stain or damage some fabrics, materials or surfaces

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3.0%, Homosalate 15.0%, Octisalate 5.0%, Octocrylene 10%, Oxybenzone 3.0%

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

​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 doctor if​

OTC - STOP USE SECTION

  • 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

• apply liberally 15 minutes before sun exposure

• reapply:
• after 80 minutes of swimming or sweating
• immediately after towel drying
• at least every 2 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 value 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-sleeved shirts, pants, hats, and sunglasses

• children under 6 months: Ask a doctor

Other information

STORAGE AND HANDLING SECTION

• protect the product in this container from excessive heat and direct sun

• may stain or damage some fabrics, materials or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

paraffin, C12-15 alkyl benzoate, octyldodecyl neopentanoate, adipic acid/diglycol crosspolymer, ozokerite, beeswax, dimethicone, neopentyl glycol diethylhexanoate, neopentyl glycol diisostearate, caprylyl glycol, BHT, fragrance

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CVS59076EFCVS59076EF

CVS26777EFCVS26777EF

CVS50300EFCVS50300EF

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69842-14969842-149-28

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
CERESINQ1LS2UJO3AIACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
PARAFFINI9O0E3H2ZEIACT
ADIPIC ACID/DIGLYCOL CROSSPOLYMER (20000 MPA.S)R9TPS68K19IACT
WHITE WAX7G1J5DA97FIACT
OCTYLDODECYL NEOPENTANOATEX8725R883TIACT
DIMETHICONE92RU3N3Y1OIACT
NEOPENTYL GLYCOL DIETHYLHEXANOATEU68ZV6W62CIACT
NEOPENTYL GLYCOL DIISOSTEARATE4M6OQ34JWWIACT
CAPRYLYL GLYCOL00YIU5438UIACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
OXYBENZONE95OOS7VE0YACTIB
OCTOCRYLENE5A68WGF6WMACTIB
HOMOSALATEV06SV4M95SACTIB
AVOBENZONEG63QQF2NOXACTIB
OCTISALATE4X49Y0596WACTIB

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
2514214e-e378-e064-e063-6394a90a1ca547a631a0-3836-28ae-e054-00144ff88e882024-10-22WarningsExact identifier
spl set id: 47a631a0-3836-28ae-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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