Jafra Sun spray on sunscreen broad spectrum SPF 50

Manufacturer
Distribuidora Comercial Jafra, S.A. de C.V. | Jafra cosmetics international Inc.
Effective date
2025-10-21
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-06-01 01:40:31

Label at a glance#

ProductJafra Sun sunscreen broad spectrum SPF 50
Active ingredientAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients Purpose

Avobenzone 3% Sunscreen

Homosalate 10% Sunscreen

Octisalate 5% Sunscreen

Octocrylene 10% Sunscreen

OTC - PURPOSE SECTION

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.

WARNINGS SECTION

Warnings

  • For external use only
  • Do not useon damaged or broken skin
  • When using this productkeep out of eyes. Rinse with water to remove.
  • Stop use and ask a doctor if rash occurs
  • Keep out of reach of children.If swallowed, get medical help or contact a poison Control Center right away

DOSAGE & ADMINISTRATION SECTION

Directions

  • Apply liberally and evenly 15 minutes before sun exposure
  • reapply:

    • after 40 minutes of swimming or sweating
    • immediately after towel drying
    • at least every 2 hours

  • Children under 6 months of age: ask a doctor.
  • 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 your time in the sun, especially from 10a.m. – 2 p.m.

      • wear long-sleeved shirts, pants, hats, and sunglasses

OTHER SAFETY INFORMATION

Other information

  • protect this product from excessive heat and direct sun

INACTIVE INGREDIENT SECTION

Inactive Ingredients

Water, Butyloctyl Salicylate, Polyester-8, Styrene/Acrylates Copolymer, Ethylhexyl Methoxycrylene, Polyester-5, Glycerin, Phenoxyethanol, Dimethicone, Bisabolol, Polysorbate 20, Potassium Cetyl Phosphate, Caprylyl Glycol, Butyrospermum Parkii (Shea) Butter, Tocopheryl Acetate, Fragrance, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Ethylhexylglycerin, Hexylene Glycol, Disodium EDTA, Triethanolamine, Benzyl Salicylate , Coumarin, Butylphenyl Methylpropional, Sodium Silicoaluminate, Linalool, Hydroxycitronellal, Limonene, Sambucus Nigra Fruit Extract

SPL UNCLASSIFIED SECTION

Questions?Call 1-800-551-2345 or visit www.jafra.com

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage description

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68828-296-01Jafra Sun sunscreen broad spectrum SPF 50125 mL in 1 BOTTLE, SPRAYSPRAY1257

Products#

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

DailyMed product names page 1 of 1 · 33 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68828-29668828-296-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 31 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
62024-12-26full-release2026-06-01 00:49:16

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
Jafra Sun sunscreen broad spectrum SPF 50AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENEDistribuidora Comercial Jafra, S.A. de C.V.b9316e16-c571-4a5c-e053-2995a90ac6a82025-10-21WarningsExact identifier
ndc (package): 68828-296-01
ndc (product): 68828-296
ndc11 (package): 68828029601
spl id: 41ad73b9-2d59-b25a-e063-6394a90a296f
spl set id: b9316e16-c571-4a5c-e053-2995a90ac6a8

Reported adverse events (FAERS/openFDA)#

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