CVS Pharmacy SPF 30 Wet & Dry Spray

Manufacturer
CVS Pharmacy
Effective date
2022-11-01
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:50:00

Label at a glance#

ProductCVS Pharmacy SPF 30 Wet and Dry
Active ingredientAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE
Label structure13 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 hold can 4-6 inches away from body, spray evenly to ensure complete coverage do not spray into face. Spray into hand and apply to face. use in well ventilated, but not windy areas 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 a...

Storage and handling

do not use near heat, flame or while smoking avoid long term storage above 104°F (40°C)

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3.0%, Homosalate 8.0%, Octisalate 4.0%, Octocrylene 8.0%, Oxybenzone 5.0%

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

FLAMMABLE

STORAGE AND HANDLING SECTION

  • do not use near heat, flame or while smoking
  • avoid long term storage above 104°F (40°C)

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.
  • do not puncture or incinerate. Contents under pressure.
  • do not store at temperatures above 120° F.

Stop use and ask a 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

INSTRUCTIONS FOR USE SECTION

  • apply liberally 15 minutes before sun exposure
  • hold can 4-6 inches away from body, spray evenly to ensure complete coverage
  • do not spray into face. Spray into hand and apply to face.
  • use in well ventilated, but not windy areas
  • 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

Inactive ingredients

INACTIVE INGREDIENT SECTION

alcohol denat., cyclopentasiloxane, octyldodecyl citrate crosspolymer, trimethylpentanediol/adipic acid/glycerin crosspolymer, ethyl methicone, bis-hydroxyethoxypropyl dimethicone, acrylates/dimethicone copolymer, fragrance, tocopheryl acetate (vitamin E), nelumbo nucifera flower extract, ascorbyl palmitate (vitamin C), retinyl palmitate (vitamin A)

Other information

SPL UNCLASSIFIED SECTION

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

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CVS78830D4CVS78830D4

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69842-13569842-135-24

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Source Document#

Source XML · Source PDF

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
2513cf84-c6bb-3688-e063-6394a90a240e6414c381-3153-370f-e053-2a91aa0a04dc2024-10-22WarningsExact identifier
spl set id: 6414c381-3153-370f-e053-2a91aa0a04dc

Reported adverse events (FAERS/openFDA)#

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