FDA.reportPublic FDA data

Sun Bum SPF 70 Premium Moisturizing Sunscreen

Manufacturer
Sun Bum, LLC
Effective date
2018-12-27
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-02 00:38:53

Label at a glance#

ProductSun Bum SPF 70 Premium Moisturizing Sunscreen
Active ingredientAVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, OCTOCRYLENE
Label structure8 sections

Indications and uses

Helps prevent sunburn. higher SPF gives more sunburn protection. 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 of 15 or higher and other sun protection measures. including: Limit time in the su...

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3.00%, Homosalate 10.00%, Octinoxate 5.00%, Octisalate 5.00%, Octocrylene 10.00%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

  • Helps prevent sunburn.
  • higher SPF gives more sunburn protection.
  • 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 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

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 of 15 or higher and other sun protection measures.
including:

  • Limit time in the sun, especially from 10 am - 2 pm.
  • Wear long-sleeve shirts, pants, hats, and sunglasses.
  • Children under 6 months: Ask a doctor.

Other information

SPL UNCLASSIFIED SECTION

  • Protect this product from excessive heat and direct sun.

​Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Beeswax, Hydrated Silica, Acrylates/C12-22 Alkyl Methacrylate Copolymer, Caprylyl Methicone, Styrene/Acrylates Copolymer, Cetyl Dimethicone, Glyceryl Stearate, PEG-100 Stearate, Polyester-8, Trideceth-6, Dimethicone, Ethylhexyl Stearate, Fragrance, Dimethyl Capramide, Sodium Polyacrylate, Ethylhexylglycerin, Trimethylsiloxysilicate, Xanthan Gum, BHT, Dipotassium Glycyrrhizate, Polyaminopropyl Biguanide, Tocopheryl Acetate, Disodium EDTA, Methylisothiazolinone.

Questions or Comments?

OTC - QUESTIONS SECTION

Call + 1 (877) 978-6286

Product Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SPF70_88mLSPF70_88mL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69039-223-012022-02-05C16284748780-1d6a99b39-6a24-a426-e053-dadaa90af4c2Sun Bum SPF 70 Premium Moisturizing Sunscreen
69039-223-012022-01-28C16284748780-1d6a99b39-6a24-a426-e053-dadaa90af4c2Sun Bum SPF 70 Premium Moisturizing Sunscreen

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69039-22369039-223-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
YELLOW WAX2ZA36H0S2VIACT
HYDRATED SILICAY6O7T4G8P9IACT
CAPRYLYL TRISILOXANEQ95M2P1KJLIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
PEG-100 STEARATEYD01N1999RIACT
TRIDECETH-63T5PCR2H0CIACT
DIMETHICONE92RU3N3Y1OIACT
ETHYLHEXYL STEARATEEG3PA2K3K5IACT
DIMETHYL CAPRAMIDEO29Y6X2JEZIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
XANTHAN GUMTTV12P4NEEIACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
GLYCYRRHIZINATE DIPOTASSIUMCA2Y0FE3FXIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
AVOBENZONEG63QQF2NOXACTIB
HOMOSALATEV06SV4M95SACTIB
OCTINOXATE4Y5P7MUD51ACTIB
OCTISALATE4X49Y0596WACTIB
OCTOCRYLENE5A68WGF6WMACTIB

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
d7405745-5f9c-9e33-e053-2995a90af34a57bfabaf-35aa-494f-b6ec-4df695fb71b72022-02-05WarningsExact identifier
spl set id: 57bfabaf-35aa-494f-b6ec-4df695fb71b7

Reported adverse events (FAERS/openFDA)#

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