Glo Skin

Manufacturer
Glo Skin Beauty
Effective date
2025-11-13
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 01:16:17

Label at a glance#

ProductGlo Skin
Active ingredientZINC OXIDE, TITANIUM DIOXIDE
Label structure8 sections

Label contents#

Full prescribing information#

Glo Skin

DOSAGE & ADMINISTRATION SECTION

Dosage and AdministrationDosage and Administration

Glo Skin

INACTIVE INGREDIENT SECTION

Inactive ingredientsInactive ingredients

Glo Skin

INDICATIONS & USAGE SECTION

Indications & usageIndications & usage

Glo Skin

OTC - ACTIVE INGREDIENT SECTION

Active IngredientsActive Ingredients

Glo Skin

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of childrenkeep out of reach of children

Glo Skin

OTC - PURPOSE SECTION

purposepurpose

Glo Skin

WARNINGS SECTION

Warning LabelWarning Label

Glo Skin

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDPPDP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60541-0391-1Glo Skin50 mL in 1 BOTTLELOTION505
60541-0391-2Glo Skin1 in 1 CARTONLOTION15

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
60541-039160541-0391-1, 60541-0391-2

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
Glo SkinTITANIUM DIOXIDE, ZINC OXIDEGlo Skin Beautyf4bed574-68c1-0d2c-e053-2a95a90a15ff2025-11-13WarningsExact identifier
ndc (package): 60541-0391-1
ndc (package): 60541-0391-2
ndc (product): 60541-0391
ndc11 (package): 60541039102
ndc11 (package): 60541039101
spl id: 437fcace-4b77-b891-e063-6294a90ac3cb
spl set id: f4bed574-68c1-0d2c-e053-2a95a90a15ff

Reported adverse events (FAERS/openFDA)#

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