CALLIEL Tinted Glow SPF 50

Manufacturer
CALLIEL PHARMA KOZMETIK SANAYI VE TICARET ANONIM SIRKETI | MADDY GLOBAL LLC
Effective date
2026-02-06
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:45:55

Label at a glance#

ProductCALLIEL Tinted Glow SPF 50 Medium
Active ingredientTITANIUM DIOXIDE, AVOBENZONE, ZINC OXIDE, OCTINOXATE
Label structure10 sections

Indications and uses

• helps prevent sunburn • if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

Dosage and administration

• apply liberally 15 minutes before sun exposure • reapply: • after 80 minutes of swimming or sweating • immediately after towel drying • at least every 2 hours • children under 6 months: Ask a doctor Sun Protection Measures: Spending time in the sun increases your risk of skin cancer and early skin aging caused by the sun. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF 15 or higher and...

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 7%
Titanium Dioxide 3.5%
Avobenzone 3.5%
Octinoxate 7%

Uses

INDICATIONS & USAGE SECTION

• helps prevent sunburn
• if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin

OTC - STOP USE SECTION

Stop use and ask a doctor if rash occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• apply liberally 15 minutes before sun exposure
• reapply:
• after 80 minutes of swimming or sweating
• immediately after towel drying
• at least every 2 hours
• children under 6 months: Ask a doctor

Sun Protection Measures: Spending time in the sun increases your risk of skin cancer and early skin aging caused by the sun. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF 15 or higher and other sun protection measures including:
• limit time in the sun, especially from 10 a.m. – 2 p.m.
• wear long-sleeve shirts, pants, hats, and sunglasses

Warnings

WARNINGS SECTION

For external use only

Purpose

OTC - PURPOSE SECTION

Sunscreen

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Caprylic/Capric Triglyceride, Butyrospermum Parkii Butter, C12-15 Alkyl Benzoate, Dimethicone, Glycerin, Propylene Glycol, Isopropyl Myristate, Cyclopentasiloxane, Acrylates/Dimethicone Copolymer, Xylitylglucoside, Phenoxyethanol, PEG-10 Dimethicone, Iron Oxides, Disteardimonium Hectorite, Anhydroxylitol, Xylitol, Aloe Barbadensis Leaf Extract, Caprylyl Glycol, Triethoxycaprylylsilane

Front Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

tintglowtintglow

lightlightmediummedium

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87411-0001-1CALLIEL Tinted Glow SPF 5050 g in 1 TUBECREAM502
87411-0002-1CALLIEL Tinted Glow SPF 50 Medium32 g in 1 TUBECREAM322
87411-0003-1CALLIEL Tinted Glow SPF 50 Light32 g in 1 TUBECREAM322

Products#

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

DailyMed product names page 1 of 1 · 30 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87411-000187411-0001-1
87411-000287411-0002-1
87411-000387411-0003-1

Ingredients#

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

DailyMed ingredient rows page 1 of 2 · 78 matching rows.

Name, UNII, Kind table
NameUNIIKind
2-ETHYLHEXYL ACRYLATE, METHACRYLATE, METHYL METHACRYLATE, OR BUTYL METHACRYLATE/HYDROXYPROPYL DIMETHICONE COPOLYMER (30000-300000 MW)S7ZA3CCJ4MIACT
TITANIUM DIOXIDE15FIX9V2JPACTIB
CAPRYLIC/CAPRIC TRIGLYCERIDEC9H2L21V7UIACT
AVOBENZONEG63QQF2NOXACTIB
CI 77492EX438O2MRTIACT
GLYCERINPDC6A3C0OXIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
CI 77499XM0M87F357IACT
PROPYLENE GLYCOL6DC9Q167V3IACT
ZINC OXIDESOI2LOH54ZACTIB
BIS-PEG-10 DIMETHICONE/DIMER DILINOLEATE COPOLYMERCF5W1YCX11IACT
XYLITYLGLUCOSIDEO0IEZ166FBIACT
ANHYDROXYLITOL8XWR7NN42FIACT
BUTYROSPERMUM PARKII (SHEA) BUTTERK49155WL9YIACT
DIMETHICONE92RU3N3Y1OIACT
C12-15 ALKYL BENZOATEA9EJ3J61HQIACT
XYLITOLVCQ006KQ1EIACT
DISTEARDIMONIUM HECTORITEX687XDK09LIACT
CI 774911K09F3G675IACT
WATER059QF0KO0RIACT
PHENOXYETHANOLHIE492ZZ3TIACT
ALOE BARBADENSIS LEAF JUICERUE8E6T4NBIACT
TRIETHOXYCAPRYLYLSILANELDC331P08EIACT
OCTINOXATE4Y5P7MUD51ACTIB
CAPRYLYL GLYCOL00YIU5438UIACT
CYCLOPENTASILOXANE0THT5PCI0RIACT
2-ETHYLHEXYL ACRYLATE, METHACRYLATE, METHYL METHACRYLATE, OR BUTYL METHACRYLATE/HYDROXYPROPYL DIMETHICONE COPOLYMER (30000-300000 MW)S7ZA3CCJ4MIACT
TITANIUM DIOXIDE15FIX9V2JPACTIB
CAPRYLIC/CAPRIC TRIGLYCERIDEC9H2L21V7UIACT
AVOBENZONEG63QQF2NOXACTIB
CI 77492EX438O2MRTIACT
GLYCERINPDC6A3C0OXIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
CI 77499XM0M87F357IACT
PROPYLENE GLYCOL6DC9Q167V3IACT
ZINC OXIDESOI2LOH54ZACTIB
BIS-PEG-10 DIMETHICONE/DIMER DILINOLEATE COPOLYMERCF5W1YCX11IACT
XYLITYLGLUCOSIDEO0IEZ166FBIACT
ANHYDROXYLITOL8XWR7NN42FIACT
BUTYROSPERMUM PARKII (SHEA) BUTTERK49155WL9YIACT

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
59dda149-7c8f-fb71-e063-6394a90ac43849f40335-e6a8-f5bc-e063-6294a90a02af2026-08-25WarningsExact identifier
spl set id: 49f40335-e6a8-f5bc-e063-6294a90a02af

Reported adverse events (FAERS/openFDA)#

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