FDA.reportPublic FDA data

MooGoo Natural Sunscreen SPF 30

Manufacturer
MooGoo USA LLC
Effective date
2020-04-16
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:34:17

Label at a glance#

ProductMooGoo Natural Sunscreen SPF 30
Active ingredientZINC OXIDE
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Zinc Oxide 25%

OTC - PURPOSE SECTION

Purpose

Sunscreen

INDICATIONS & USAGE 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 use on damaged or broken skin
  • When using this product keep out of eyes
  • Rinse with water to remove
  • Stop use and ask a doctor if rash occurs
  • Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

DOSAGE & ADMINISTRATION SECTION

Directions

  • Apply liberally 15 minutes before sub exposure
  • Reapply
  • After 40 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 - 2pm - Wear long-sleeve shirts, pants, hats, and sunglasses
  • Children under 6 months. Ask a doctor

OTHER SAFETY INFORMATION

Other Information

  • Store below 86F or 30C
  • Protect the product in this container from excessive heat and direct sun

INDICATIONS & USAGE SECTION

Inactive Ingredients

Beeswax,Capryl Glycol, Cetyl Phosphate, Coco Caprylate, Galactoarabinan, Glycerin. Jojoba Oil, Lecithin, Oleic Acid, Polyglyceryl-2 Dipolyhydroxystearate, Polyglyceryl-3 Polyricinoleate, Sodium Chloride (salt), Sorbitan Olivate, Tropolone, Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69788-00369788-003-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
POLYGLYCERYL-3 RICINOLEATEMZQ63P0N0WIACT
CAPRYLYL GLYCOL00YIU5438UIACT
GLYCERINPDC6A3C0OXIACT
LECITHIN, SOYBEAN1DI56QDM62IACT
WHITE WAX7G1J5DA97FIACT
POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE9229XJ4V12IACT
GALACTOARABINANSL4SX1O487IACT
TROPOLONE7L6DL16P1TIACT
POLYHYDROXYSTEARIC ACID (2300 MW)YXH47AOU0FIACT
1,2-HEXANEDIOLTR046Y3K1GIACT
COCO-CAPRYLATE/CAPRATE8D9H4QU99HIACT
ZINC OXIDESOI2LOH54ZACTIM
SORBITAN OLIVATEMDL271E3GRIACT
SIMMONDSIA CHINENSIS SEEDD24K2Q1F6HIACT

Source Document#

Source XML · Source PDF

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
d0eebc4c-556b-3332-e053-2995a90a5e96a36f692d-5b3d-105f-e053-2995a90a234e2021-11-16WarningsExact identifier
spl set id: a36f692d-5b3d-105f-e053-2995a90a234e

Reported adverse events (FAERS/openFDA)#

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