FDA.reportPublic FDA data

hers mineral sunscreen multi-screen

Manufacturer
HIMS | Nanophase Technologies Corporation
Effective date
2024-10-07
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 20:53:16

Label at a glance#

Producthers mineral sunscreen multi-screen
Active ingredientZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

hers mineral sunscreen multi-screen

DOSAGE & ADMINISTRATION SECTION

Dosage and AdministrationDosage and Administration

hers mineral sunscreen multi-screen

INACTIVE INGREDIENT SECTION

Inactive ingredientsInactive ingredients

hers mineral sunscreen multi-screen

INDICATIONS & USAGE SECTION

Indications & usageIndications & usage

hers mineral sunscreen multi-screen

OTC - ACTIVE INGREDIENT SECTION

Active IngredientsActive Ingredients

hers mineral sunscreen multi-screen

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of childrenkeep out of reach of children

hers mineral sunscreen multi-screen

OTC - PURPOSE SECTION

purposepurpose

hers mineral sunscreen multi-screen

WARNINGS SECTION

Warning LabelWarning Label

hers mineral sunscreen multi-screen

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDPPDP

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71730-901HERS MINERAL SUNSCREEN MULTI-SCREEN (ZINC OXIDE) LOTION [HIMS]3Legacy NDC20241009_deede344-b738-58d8-e053-2a95a90a566f.zip

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71730-90171730-901-01, 71730-901-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 23 matching rows.

Name, UNII, Kind table
NameUNIIKind
LECITHIN, SOYBEAN1DI56QDM62IACT
POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE9229XJ4V12IACT
HYDROLYZED JOJOBA ESTERS (ACID FORM)UDR641JW8WIACT
METHYLPROPANEDIOLN8F53B3R4RIACT
CAPRYLYL GLYCOL00YIU5438UIACT
PHENYLPROPANOL0F897O3O4MIACT
XANTHAN GUMTTV12P4NEEIACT
ISOAMYL LAURATEM1SLX00M3MIACT
HEXYLENE GLYCOLKEH0A3F75JIACT
TOCOPHEROLR0ZB2556P8IACT
CETYL ALCOHOL936JST6JCNIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
GLYCERINPDC6A3C0OXIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
WATER059QF0KO0RIACT
.ALPHA.-BISABOLOL, (+)-105S6I733ZIACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
CETETH-20I835H2IHHXIACT
PULLULAN8ZQ0AYU1TTIACT
SQUALANEGW89575KF9IACT
STEARETH-20L0Q8IK9E08IACT
ZINC OXIDESOI2LOH54ZACTIB
CYCLODEXTRINS7E6SK9QDT8IACT

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
23e37215-5235-b1a0-e063-6294a90a20eddeede344-b738-58d8-e053-2a95a90a566f2024-10-07WarningsExact identifier
spl id: 23e37215-5235-b1a0-e063-6294a90a20ed
spl set id: deede344-b738-58d8-e053-2a95a90a566f

Reported adverse events (FAERS/openFDA)#

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