FDA.reportPublic FDA data

Zebs broad spectrum sunscreen

Manufacturer
New Era Naturals LLC
Effective date
2016-01-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:44:54

Label at a glance#

ProductZebs broad spectrum sunscreen
Active ingredientZINC OXIDE
Label structure6 sections

Label contents#

Full prescribing information#

see label

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

labellabel

INACTIVE INGREDIENT SECTION

inactive ingredientsinactive ingredients

INSTRUCTIONS FOR USE SECTION

instructions for useinstructions for use

OTC - ACTIVE INGREDIENT SECTION

active ingredientactive ingredient

OTC - WHEN USING SECTION

when usingwhen using

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Zebs display panelZebs display panel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70397-2016-12020-01-31C16284748780-19d75b9d0-7732-f424-e053-dadaa90a57ceZebs Organics-20 SPF broad spectrum sunscreen
70397-2016-22020-01-31C16284748780-19d75b9d0-7732-f424-e053-dadaa90a57ceZebs Organics-20 SPF broad spectrum sunscreen

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70397-2016-1Zebs broad spectrum sunscreen88.4 g in 1 TUBELOTION88.41
70397-2016-2Zebs broad spectrum sunscreen208 g in 1 TUBELOTION2081

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70397-2016ZEBS BROAD SPECTRUM SUNSCREEN (ZINC OXIDE) LOTION [NEW ERA NATURALS LLC]1Legacy NDC, 2 package rows20160208_289542c1-1347-3b43-e054-00144ff8d46c.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70397-201670397-2016-1, 70397-2016-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
ZINC OXIDESOI2LOH54ZACTIB
SUNFLOWER OIL3W1JG795YIIACT
COCONUT OILQ9L0O73W7LIACT
WHITE WAX7G1J5DA97FIACT
OLIVE OIL6UYK2W1W1EIACT
SHEA BUTTERK49155WL9YIACT

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
289542c1-1348-3b43-e054-00144ff8d46c289542c1-1347-3b43-e054-00144ff8d46c2016-01-29Exact identifier
spl id: 289542c1-1348-3b43-e054-00144ff8d46c
spl set id: 289542c1-1347-3b43-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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