SUNCEUTICAL SPF 50 MINERAL GLOW SERUM- zinc oxide cream

Sunceutical SPF 50 Mineral Glow Serum by

Drug Labeling and Warnings

Sunceutical SPF 50 Mineral Glow Serum by is a Otc medication manufactured, distributed, or labeled by Baxter Laboratories Pty. Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient Purpose

Zinc Oxide 20% Suncreen

PURPOSE

Uses

• Helps prevent
• If used as directed with other sun protect measures ( see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

KEEP OUT OF REACH OF CHILDREN

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

INDICATIONS & USAGE

Stop use and ask a doctor if rash occurs.

WARNINGS

Warnings

• For external use only
• Do not use on damaged or broken skin
• When using this product keep out of eyes. Rinse with water to remove.

DOSAGE & ADMINISTRATION

Directions

• Apply liberally 15 minutes before sun exposure
• Children under 6 months of age: Ask a doctor
• Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
• Limit time in the sun, especially from 10 a.m. - 2 p.m.
• Wear long-sleeved shirts, pants, hats, and sunglasses
• Reapply at least every 2 hours
• Use a water resistant sunscreen if swimming or sweating

OTHER SAFETY INFORMATION

Other information

• Protect the product in the container from excessive heat and direct

INACTIVE INGREDIENT

Inactive ingredients

Water, Coco-Caprylate/Caprate, Isohexadecane, Caprylic/Capric Triglyceride, Coco-Caprylate, Polyglyceryl-2 Dipolyhydroxystearate, Isoamyl Laurate, Pentylene Glycol, Isododecane, Polyglyceryl-3 Polyricinoleate, Mica, Glyceryl Polymethacrylate, Polyglyceryl-3 Diisostearate, Sorbitan Olivate, Titantium Dioxide Iron Oxides, Magnesium Sulfate, Polyhydroxystearic Acid, Saccharide Isomerate, Isostearic Acid, Fragrance, Disteardimonium Hectorite, Hydroxyacetophenone, Propylene Glycol, Pongamia Pinnata Seed Extract, Propylene Carbonate, Limonene, Citric Acid, Sodium Citrate, Linalool, Palmitoyl Tripeptide-1

PRINCIPAL DISPLAY PANEL

Emma Lewisham

Sunceutical SPF 50 Mineral Glow Serum

Zinc Oxide Mineral Sun-Active

Broad Spectrum SPF 50 Sunscreen

30mL/ 1 FL. OZ.

INGREDIENTS AND APPEARANCE

SUNCEUTICAL SPF 50 MINERAL GLOW SERUM 
zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70157-367
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	20 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
IRON OXIDES (UNII: 1K09F3G675)
POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
WATER (UNII: 059QF0KO0R)
COCO-CAPRYLATE (UNII: 4828G836N6)
SORBITAN OLIVATE (UNII: MDL271E3GR)
ISOSTEARIC ACID (UNII: X33R8U0062)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CITRIC ACID (UNII: 2968PHW8QP)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
ISOHEXADECANE (UNII: 918X1OUF1E)
CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)
ISOAMYL LAURATE (UNII: M1SLX00M3M)
MICA (UNII: V8A1AW0880)
POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)
LIMONENE, (+/-)- (UNII: 9MC3I34447)
PALMITOYL TRIPEPTIDE-1 (UNII: RV743D216M)
SACCHARIDE ISOMERATE (UNII: W8K377W98I)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
MAGNESIUM SULFATE (UNII: DE08037SAB)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
ISODODECANE (UNII: A8289P68Y2)
GLYCERYL POLYMETHACRYLATE (300000 MPA.S) (UNII: 2B25A5KAD6)
PONGAMIA PINNATA SEED (UNII: C2BRV53B1V)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
POLYGLYCERYL-3 PENTARICINOLEATE (UNII: 7Q0OK5DOT4)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70157-367-02	1 in 1 CARTON	01/20/2025
1	NDC: 70157-367-01	30 mL in 1 JAR; Type 0: Not a Combination Product
2	NDC: 70157-367-04	1 in 1 CARTON	01/20/2025
2	NDC: 70157-367-03	30 mL in 1 CUP; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	01/20/2025

Labeler - Baxter Laboratories Pty. Ltd. (740537709)