FDA.reportPublic FDA data

Essentials D42.000/D42AA R1 Sunscreen Spray for Kids SPF 50

Manufacturer
Amazon.com Services LLC | Nice-Pak Products, LLC
Effective date
2026-02-26
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:47:43

Label at a glance#

ProductAvebonzone, Homosalate, Octisalate
Active ingredientHOMOSALATE, OCTISALATE, AVOBENZONE
Label structure14 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

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...

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3%
Homosalate 12%
Octisalate 5%

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: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 puncture or incinerate. Do not store at temperature above 120ºF.

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

OTHER SAFETY INFORMATION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

Disclaimers

SPL UNCLASSIFIED SECTION

May stain or damage some fabrics or surfaces

**This product is not manufactured or distributed by Beiersdorf AG, distributor of Coppertone ®Sunscreen Spray Kids Broad Spectrum SPF 50.

Adverse Reaction

ADVERSE REACTIONS SECTION

Made in USA with US and foreign components.

DISTRIBUTED BY: AMAZON.COM SERVICES LLC

SEATTLE, WA 98109 1-877-485-0385

©2026 AMAZON.COM INC. OR ITS AFFILIATES.

ALL RIGHTS RESERVED.

WWW.AMAZON.COM/AMAZONESSENTIALS

METAL CAN

Check Locally*

*Not recycled in all communities.

how2recycle.info

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

amazon essentials

SPF 50 

Kids Sunscreen Spray

Moisturizing

Broad spectrum SPF 50

Water resistant (80 minutes)

Formulated without phthalates, PABA, dyes, octinoxate, octocrylene or oxybenzone

Hypoallergenic

Compare to Coppertone ®Sunscreen Spray Kids Broad Spectrum SPF 50**

NET WT 5.5 OZ (156 g)

image descriptionimage description

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72288-942-14Avebonzone, Homosalate, Octisalate156 g in 1 CANSPRAY1562

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72288-94272288-942-14

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
DIETHYLHEXYL 2,6-NAPHTHALATEI0DQJ7YGXMIACT
DIISOPROPYL ADIPATEP7E6YFV72XIACT
ACRYLATE/ISOBUTYL METHACRYLATE/N-TERT-OCTYLACRYLAMIDE COPOLYMER (40000 MW)7LL6SY9YFVIACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
NEOPENTYL GLYCOL DIHEPTANOATE5LKW3C543XIACT
.ALPHA.-AMYLCINNAMALDEHYDEWC51CA3418IACT
HYDROXYCITRONELLAL8SQ0VA4YURIACT
LINALOOL, (+/-)-D81QY6I88EIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
HOMOSALATEV06SV4M95SACTIB
OCTISALATE4X49Y0596WACTIB
AVOBENZONEG63QQF2NOXACTIB

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
Avebonzone, Homosalate, OctisalateAVEBONZONE, HOMOSALATE, OCTISALATEAmazon.com Services LLC4ab66c16-5f4c-6987-e063-6294a90add862026-02-26Warnings, Adverse reactionsExact identifier
ndc (package): 72288-942-14
ndc (product): 72288-942
ndc11 (package): 72288094214
spl id: 4bbec5b6-e92e-5533-e063-6294a90a9af6
spl set id: 4ab66c16-5f4c-6987-e063-6294a90add86

Reported adverse events (FAERS/openFDA)#

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