FDA.reportPublic FDA data

Blume Sunburst Sunscreen

Manufacturer
Blume
Effective date
2026-05-21
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:58:25

Label at a glance#

ProductBlume Sunburst Sunscreen
Active ingredientZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

Blume Sunburst Sunscreen

DOSAGE & ADMINISTRATION SECTION

Dosage and AdministrationDosage and Administration

Blume Sunburst Sunscreen

INACTIVE INGREDIENT SECTION

Inactive ingredientsInactive ingredients

Blume Sunburst Sunscreen

INDICATIONS & USAGE SECTION

Indications & usageIndications & usage

Blume Sunburst Sunscreen

OTC - ACTIVE INGREDIENT SECTION

Active IngredientsActive Ingredients

Blume Sunburst Sunscreen

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of childrenkeep out of reach of children

Blume Sunburst Sunscreen

OTC - PURPOSE SECTION

purposepurpose

Blume Sunburst Sunscreen

WARNINGS SECTION

Warning LabelWarning Label

Blume Sunburst Sunscreen

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDPPDP

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
684ea482-2e8b-14af-5664-b98f1e402036Product name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
b060cc1a-fe47-856b-0b77-4448b5963de8Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83656-2106-1Blume Sunburst Sunscreen50 mL in 1 BOTTLELOTION504
83656-2106-2Blume Sunburst Sunscreen1 in 1 CARTONLOTION14

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
83656-210683656-2106-1, 83656-2106-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 31 matching rows.

Name, UNII, Kind table
NameUNIIKind
FERRIC OXIDE YELLOWEX438O2MRTIACT
PHENYLPROPANOL0F897O3O4MIACT
STEARALKONIUM HECTORITEOLX698AH5PIACT
FERRIC OXIDE RED1K09F3G675IACT
CENTELLA ASIATICA LEAF6810070TYDIACT
JOJOBA OIL724GKU717MIACT
ORYZA SATIVA WHOLE84IVV0906ZIACT
TRIDECYL SALICYLATEAZQ08K38Z1IACT
SILICON DIOXIDEETJ7Z6XBU4IACT
TOCOPHEROLR0ZB2556P8IACT
CAPRYLYL GLYCOL00YIU5438UIACT
COCO-CAPRYLATE4828G836N6IACT
NYLON-12446U8J075BIACT
LECITHIN, SOYBEAN1DI56QDM62IACT
METHYLPROPANEDIOLN8F53B3R4RIACT
POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE9229XJ4V12IACT
ALLANTOIN344S277G0ZIACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
ROSMARINUS OFFICINALIS FLOWERNR1A27F29OIACT
.ALPHA.-BISABOLOL, (+)-105S6I733ZIACT
ZINC OXIDESOI2LOH54ZACTIB
SODIUM HYDROXIDE55X04QC32IIACT
WATER059QF0KO0RIACT
NIACINAMIDE25X51I8RD4IACT
PROPANEDIOL5965N8W85TIACT
TETRASODIUM GLUTAMATE DIACETATE5EHL50I4MYIACT
SODIUM CHLORIDE451W47IQ8XIACT
POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/SEBACATE687U3PEB2YIACT
POLYGLYCERYL-3 DIISOSTEARATE46P231IQV8IACT
RUTIN5G06TVY3R7IACT
FERROSOFERRIC OXIDEXM0M87F357IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
32025-10-15monthly-update2026-06-03 17:39:44
22025-08-13full-release2026-06-01 01:10:19

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
Blume Sunburst SunscreenZINC OXIDEBlume21ef2c6b-8ae7-8bcf-e063-6294a90ae9e12026-05-21WarningsExact identifier
ndc (package): 83656-2106-2
ndc (package): 83656-2106-1
ndc (product): 83656-2106
ndc11 (package): 83656210602
ndc11 (package): 83656210601
spl id: 52579ad4-ad8a-3a6b-e063-6294a90a2844
spl set id: 21ef2c6b-8ae7-8bcf-e063-6294a90ae9e1

Reported adverse events (FAERS/openFDA)#

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