Sunnyscreen SPF Lotion of Babies + kiddos

Manufacturer
Supergoop, LLC
Effective date
2023-12-14
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 00:04:23

Label at a glance#

ProductSunnyscreen SPF 50
Active ingredientTITANIUM DIOXIDE, ZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients Purpose

TItanium Dioxide 3.4% Sunscreen

Zinc Oxide 23.8% 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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

If product is swallowed, get medical help or contact a poison Control Center right away

INDICATIONS & USAGE SECTION

Stop use and ask a doctor if rash occurs or irritation develops and lasts.

WARNINGS SECTION

Warnings

Do not use on damaged or broken skin

When using this product keep out of eyes. Rinse with water to remove

For external use only

DOSAGE & ADMINISTRATION SECTION

Directions

  • Apply liberally and generously 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 value of 15 or higher and other sun
protection measures including:

  • limit your 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.

INACTIVE INGREDIENT SECTION

Avena Sativa (Oat) Kernel Flour, Butyloctyl Salicylate, Butyrospermum Parkii (Shea) Butter, C9-12 Alkane, Caesalpinia Spinosa Gum, Calendula Officinalis Flower Extract, Caprylhydroxamic Acid, Caprylic/Capric Triglyceride,Cetearyl Alcohol,Chamomila Recutita (Matricaria) Flower Extract, Coco-Caprylate/Caprate, Ethylhexylglycerin, Glycerin, Glyceryl Caprylate, Glyceryl Stearate, Haematococcus Pluvialis Extract, Helianthus Annuus (Sunflower) Seed Oil, Hydrolyzed Jojoba Esters, Jojoba Esters, Methyl Dihydroabietate, Myrciaria Dubia Fruit Extract, Polyhydroxystearic Acid, Propanediol, Sea Water, Silica, Sodium Phytate, Sorbitan Stearate, Sorbityl Laurate, Stearic Acid, Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Sunnyscreen SPF 50 Lotion for babies+ Kiddos

3 fl. oz./ 89 ml

TubeTube

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75936-250-01Sunnyscreen SPF 5089 mL in 1 BOTTLELOTION896
75936-250-02Sunnyscreen SPF 505 mL in 1 PACKETLOTION56

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75936-250SUNNYSCREEN SPF 50 (TITANIUM DIOXIDE, ZINC OXIDE) LOTION [SUPERGOOP, LLC]6Legacy NDC, 2 package rows20231215_857ef2e1-31da-7647-e053-2991aa0a94f5.zip

Products#

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

DailyMed product names page 1 of 1 · 32 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75936-25075936-250-01, 75936-250-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 30 matching rows.

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
0c7f1dcd-1268-bff4-e063-6294a90a74b4857ef2e1-31da-7647-e053-2991aa0a94f52023-12-14WarningsExact identifier
spl id: 0c7f1dcd-1268-bff4-e063-6294a90a74b4
spl set id: 857ef2e1-31da-7647-e053-2991aa0a94f5

Reported adverse events (FAERS/openFDA)#

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