FDA.reportPublic FDA data

SPF 30 Pure Mineral Face Body Sunscreen

Manufacturer
Mi Amore Skincare, LLC | Mi Amore Skincare LLC
Effective date
2020-04-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:07:47

Label at a glance#

ProductSPF 30 Pure Mineral Face Body Sunscreen
Active ingredientZINC OXIDE
Label structure2 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Sunscreen Face + BodySunscreen Face + Body

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SPF Face Sunscreen LabelSPF Face Sunscreen Label

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
73770-872-172022-01-28C16284748780-1d6a99b39-d749-a426-e053-dadaa90af4c2a276836b-876d-56fe-e053-2a95a90a939c
73770-872-182022-01-28C16284748780-1d6a99b39-d749-a426-e053-dadaa90af4c2a276836b-876d-56fe-e053-2a95a90a939c
73770-872-352022-01-28C16284748780-1d6a99b39-d749-a426-e053-dadaa90af4c2a276836b-876d-56fe-e053-2a95a90a939c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73770-872-17SPF 30 Pure Mineral Face Body Sunscreen103.5 mL in 1 BOTTLE, PUMPLOTION103.51
73770-872-18SPF 30 Pure Mineral Face Body Sunscreen52 mL in 1 BOTTLE, PUMPLOTION521
73770-872-35SPF 30 Pure Mineral Face Body Sunscreen103.5 mL in 1 BOTTLE, PUMPLOTION103.51

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73770-872SPF 30 PURE MINERAL FACE BODY SUNSCREEN (ZINC OXIDE) LOTION [MI AMORE SKINCARE, LLC]1Legacy NDC, 3 package rows20200425_a276836b-876d-56fe-e053-2a95a90a939c.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73770-87273770-872-35, 73770-872-17, 73770-872-18

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
JOJOBA OIL724GKU717MIACT
OLIVE OIL6UYK2W1W1EIACT
RASPBERRY SEED OIL9S8867952AIACT
BROWN IRON OXIDE1N032N7MFOIACT
PEG-80 SORBITAN PALMITATE4NR71FN0IAIACT
ZINC OXIDESOI2LOH54ZACTIB
COCONUT OILQ9L0O73W7LIACT
CETYL PALMITATE5ZA2S6B08XIACT
ALOE VERA LEAFZY81Z83H0XIACT
GREEN TEA LEAFW2ZU1RY8B0IACT
CETEARYL OLIVATE58B69Q84JOIACT
SORBITAN OLIVATEMDL271E3GRIACT

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
a276836b-876e-56fe-e053-2a95a90a939ca276836b-876d-56fe-e053-2a95a90a939c2020-04-04Exact identifier
spl id: a276836b-876e-56fe-e053-2a95a90a939c
spl set id: a276836b-876d-56fe-e053-2a95a90a939c

Reported adverse events (FAERS/openFDA)#

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