FDA.reportPublic FDA data

KidZGoo Natural Sunscreen

Manufacturer
RENU LABORATORIES, INC.
Effective date
2021-08-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:41:51

Label at a glance#

ProductKidZGoo Natural Sunscreen
Active ingredientZINC OXIDE
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Zinc Oxide

OTC - PURPOSE SECTION

Purpose

Sunscreen

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. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - STOP USE SECTION

Stop use and ask a doctor if rash occurs

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - QUESTIONS SECTION

855-KIDZGOO

Melearning Media LLC

Upper Dublin, PA

DOSAGE & ADMINISTRATION SECTION

Directions

  • apply liberally 15 minutes before sun exposure
  • reapply;
    • after 80 minutes of swimming or sweating
    • immediately after towel drying
    • at least every 2 hours

OTHER SAFETY INFORMATION

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 value of SPF 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

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.

INACTIVE INGREDIENT SECTION

Inactive Ingredients:

Benzyl Alcohol, Caprylic/Capric Triglyceride, Cetearyl Alcohol, Cetearyl Olivate, Coco-Caprylate, Dehydroacetic Acid, Deionized Water, Isostearic Acid, Lecithin, Microcrystalline Cellulose, Panthenol, Polyglyceryl-3, Polyhydroxystearic Acid, Silica, Sodium Phytate, Sorbitan Olivate, Stearyl Octyldodecyl Citrate Crosspolymer, Tocopherol, Xantan Gum

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Pouch Front and BackPouch Front and Back

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76348-650-162025-01-30C16284748780-12cef2736-818b-d83d-e063-dadaa90ab31fKidZGoo Natural Sunscreen

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76348-650-16KidZGoo Natural Sunscreen448 g in 1 POUCHLOTION4481

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76348-650KIDZGOO NATURAL SUNSCREEN (ZINC OXIDE) LOTION [RENU LABORATORIES, INC.]1Legacy NDC, 1 package rows20210812_c8c251e1-ab0b-edba-e053-2995a90abfd4.zip

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76348-65076348-650-16

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
STYRENE/ACRYLAMIDE COPOLYMER (MW 500000)5Z4DPO246AIACT
PANTHENOLWV9CM0O67ZIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
WATER059QF0KO0RIACT
PHENOXYETHANOLHIE492ZZ3TIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
PHYTATE SODIUM88496G1ERLIACT
XANTHAN GUMTTV12P4NEEIACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
POLYHYDROXYSTEARIC ACID (2300 MW)YXH47AOU0FIACT
CETEARYL OLIVATE58B69Q84JOIACT
STEARYL/OCTYLDODECYL CITRATE CROSSPOLYMERPN88NW0KPKIACT
CAPRYLYL GLYCOL00YIU5438UIACT
SORBITAN OLIVATEMDL271E3GRIACT
ZINC OXIDESOI2LOH54ZACTIB
COCO-CAPRYLATE4828G836N6IACT

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
c8c251e1-ab0c-edba-e053-2995a90abfd4c8c251e1-ab0b-edba-e053-2995a90abfd42021-08-04WarningsExact identifier
spl id: c8c251e1-ab0c-edba-e053-2995a90abfd4
spl set id: c8c251e1-ab0b-edba-e053-2995a90abfd4

Reported adverse events (FAERS/openFDA)#

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