Always Golden Daily Moisturizer (Tinted)

Manufacturer
A-Frame SunCo Inc | Nanophase Technologies Corporation
Effective date
2025-01-09
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 00:52:21

Label at a glance#

ProductAlways Golden Daily Moisturizer (Tinted)
Active ingredientTITANIUM DIOXIDE, ZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

Always Golden Daily Moisturizer (Tinted)

DOSAGE & ADMINISTRATION SECTION

Dosage and AdministrationDosage and Administration

Always Golden Daily Moisturizer (Tinted)

INACTIVE INGREDIENT SECTION

Inactive ingredientsInactive ingredients

Always Golden Daily Moisturizer (Tinted)

INDICATIONS & USAGE SECTION

Indications & usageIndications & usage

Always Golden Daily Moisturizer (Tinted)

OTC - ACTIVE INGREDIENT SECTION

Active IngredientsActive Ingredients

Always Golden Daily Moisturizer (Tinted)

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of childrenkeep out of reach of children

Always Golden Daily Moisturizer (Tinted)

OTC - PURPOSE SECTION

purposepurpose

Always Golden Daily Moisturizer (Tinted)

WARNINGS SECTION

Warning LabelWarning Label

Always Golden Daily Moisturizer (Tinted)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDPPDP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82184-1337-1Always Golden Daily Moisturizer (Tinted)28 mL in 1 BOTTLE, PUMPLOTION284
82184-1337-2Always Golden Daily Moisturizer (Tinted)1 in 1 CARTONLOTION14
82184-1337-3Always Golden Daily Moisturizer (Tinted)60 mL in 1 BOTTLELOTION604

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82184-1337ALWAYS GOLDEN DAILY MOISTURIZER (TINTED) (TITANIUM DIOXIDE, ZINC OXIDE) LOTION [A-FRAME SUNCO INC]4Legacy NDC, 3 package rows20250112_d9b62909-e61e-e60c-e053-2995a90ae713.zip

Products#

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

DailyMed product names page 1 of 1 · 38 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82184-133782184-1337-1, 82184-1337-2, 82184-1337-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 36 matching rows.

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
2b4787da-c1fb-234b-e063-6394a90ad479d9b62909-e61e-e60c-e053-2995a90ae7132025-01-09WarningsExact identifier
spl id: 2b4787da-c1fb-234b-e063-6394a90ad479
spl set id: d9b62909-e61e-e60c-e053-2995a90ae713

Reported adverse events (FAERS/openFDA)#

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