FDA.reportPublic FDA data

Care One D48.000/D48AA Sunscreen Spray SPF 30

Manufacturer
Retail Business Services, LLC | Nice-Pak Products, LLC
Effective date
2026-02-06
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:37:21

Label at a glance#

ProductBroad Spectrum Sunscreen SPF 30
Active ingredientAVOBENZONE, HOMOSALATE, OCTISALATE
Label structure16 sections

Indications and uses

helps prevent sunburn if used as directed with other sun protections measures (see Directions ), decreases the risk of skin cancer and early skin aging caused by the sun

Dosage and administration

spray liberally and spread evenly by hand 15 minutes before sun exposure apply to all skin exposed to the sun hold container 4 to 6 inches from the skin to apply do not spray directly into face. Spray on hands then apply to face. do not apply in windy conditions use in a well-ventilated area and avoid inhalation reapply: after 80 minutes of swimming or sweating immediately after towel drying at least every 2 hours...

Storage and handling

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

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3%

Homosalate 10%

Octisalate 5%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

  • helps prevent sunburn
  • if used as directed with other sun protections 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:

OTHER SAFETY INFORMATION

Keep away from fire or flame.

  • after application, wait until product dries before approaching a source of heat or flame, or before smoking

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.
  • contents under pressure. Do not punture or incinerate. Do not store at temperature 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 swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • spray liberally and spread evenly by hand 15 minutes before sun exposure
  • apply to all skin exposed to the sun
  • hold container 4 to 6 inches from the skin to apply
  • do not spray directly into face. Spray on hands then apply to face.
  • do not apply in windy conditions
  • use in a well-ventilated area and avoid inhalation
  • 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 of age: Ask a doctor

Other information

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

alcohol denat., diethylhexyl 2,6-naphthalate, acrylates/octylacrylamide copolymer, diisopropyl adipate, neopentyl glycol diheptanoate, butyloctyl salicylate, fragrance, tocopheryl acetate

Questions or comments?

OTC - QUESTIONS SECTION

1-833-992-3872

Disclaimer

SPL UNCLASSIFIED SECTION

May stain or damage some fabrics or surfaces

Adverse Reaction

ADVERSE REACTIONS SECTION

DISTRIBUTED BY: ADUSA DISTRIBUTION, LLC

SALISBURY, NC 28147

For product questions or concerns, contact us at 1-833-992-3872

Quality guaranteed or your money back.

DSP-TN-21091 

DSP-MO-20087

Discard Seal, Empty & Replace Lid

METAL CAN

how2recycle.info

Principal Panel Display

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CAREONE ®

Broad Spectrum

SUNSCREEN

SPRAY

SPF 30

UVA/UVB SUNSCREEN

Broad Spectrum SPF 30

  • Contains Vitamin E
  • Dermatologist Tested
  • Water Resistant (80 min)
  • Hypoallergenic
  • Oxybenzone + Octinoxate Free

NEW WT. 5.5OZ (156 g)

image descriptionimage description

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72476-948-14Broad Spectrum Sunscreen SPF 30156 g in 1 CANSPRAY1564

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72476-94872476-948-14

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
DIETHYLHEXYL 2,6-NAPHTHALATEI0DQJ7YGXMIACT
ACRYLATE/ISOBUTYL METHACRYLATE/N-TERT-OCTYLACRYLAMIDE COPOLYMER (40000 MW)7LL6SY9YFVIACT
DIISOPROPYL ADIPATEP7E6YFV72XIACT
NEOPENTYL GLYCOL DIHEPTANOATE5LKW3C543XIACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
AVOBENZONEG63QQF2NOXACTIB
HOMOSALATEV06SV4M95SACTIB
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
Broad Spectrum Sunscreen SPF 30AVOBENZONE, HOMOSALATE, OCTISALATERetail Business Services, LLCccb651f6-e567-4c5f-9109-8767270cc4be2026-02-06Warnings, Adverse reactionsExact identifier
ndc (package): 72476-948-14
ndc (product): 72476-948
ndc11 (package): 72476094814
spl id: 4a2ccf14-7172-7fa4-e063-6294a90add87
spl set id: ccb651f6-e567-4c5f-9109-8767270cc4be

Reported adverse events (FAERS/openFDA)#

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