Daily Defence Mineral Sunscreen SPF 50+ Fragrance Free
- Manufacturer
- Ultraceuticals Pty Ltd
- Effective date
- 2026-06-16
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- daily-update
- Hydrated at
- 2026-09-01 13:02:11
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active Ingredients
Zinc Oxide 14% w/w
Purpose
Sunscreen
OTC - PURPOSE SECTION
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
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.
INDICATIONS & USAGE SECTION
Stop use and ask a doctor if
- skin rash occurs
WARNINGS SECTION
Warnings
Do not use
- on damaged or broken skin
When using this product
- keep out of eyes. Rinse with water to remove
For external use only
DOSAGE & ADMINISTRATION SECTION
Directions
- Shake well.
- apply liberally and evenly 15 minutes before sun exposure.
- reapply at least every 2 hours.
- use a water resistant sunscreen if swimming or sweating.
- 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 reduce this risk, regularly use a sunscreen with a Broad Spectrum of 15 or higer and other sun protection measures, including:
- limit time in the sun , especially between 10am-2pm.
- Wear long-sleeved shirts, pants, and sunglasses.
INACTIVE INGREDIENT SECTION
Inactive ingredients: Water, C12-15 Alkyl Benzoate, Butyloctyl Salicylate, Isododecane, Lauryl PEG-8 Dimethicone, Caprylic/Capric Triglyceride, Niacinamide, Polymethylsilsesquioxane, Propanediol, Caprylyl Methicone, Dimethicone, Methylpropanediol, Isoamyl Laurate, Tridecyl Salicylate, Polyglyceryl-2 Dipolyhydroxystearate, Sodium Chloride, Caprylyl Glycol, Bisabolol, Lecithin, Allantoin, Phenylpropanol, caffeine, Carnosine.
OTHER SAFETY INFORMATION
Other information
Protect from excessive heat and direct sun. Stand upright, cap down.
OTC - QUESTIONS SECTION
Questions?
Call 833 703 9067
Email advice@ultraceuticals.com
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Daily Defence
Ultraceuticals
Mineral Sunscreen SPF 50+ Fragrance free
75mL/ 2.54 fl. oz.
Product Linked Resources#
| Resource | Code type | Value | Equivalent identifiers | Source image |
|---|---|---|---|---|
| Barcode | EAN-13 | 9352207012333 | GTIN-13: 9352207012333 EAN-13: 9352207012333 GTIN storage (14 digits): 09352207012333 | PDM-N370-075C2_Updated-1.jpg |
Products#
Every source-derived product name is available through these pages.
- Daily Defence Mineral Sunscreen SPF 50 Fragrance Free
- Zinc Oxide
- WATER
- C12-15 ALKYL BENZOATE
- BUTYLOCTYL SALICYLATE
- ISODODECANE
- LAURYL PEG-8 DIMETHICONE (300 CPS)
- CAPRYLIC/CAPRIC TRIGLYCERIDE
- NIACINAMIDE
- POLYMETHYLSILSESQUIOXANE (11 MICRONS)
- PROPANEDIOL
- CAPRYLYL METHICONE
- DIMETHICONE
- METHYLPROPANEDIOL
- ISOAMYL LAURATE
- TRIDECYL SALICYLATE
- POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE
- SODIUM CHLORIDE
- CAPRYLYL GLYCOL
- BISABOLOL
- LECITHIN, SOYBEAN
- ALLANTOIN
- PHENYLPROPANOL
- CAFFEINE
- CARNOSINE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 10028-035 | 10028-035-01, 10028-035-02 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Daily Defence Mineral Sunscreen SPF 50 Fragrance Free | ZINC OXIDE | Ultraceuticals Pty Ltd | 5461ee82-0297-ce22-e063-6294a90a729b | 2026-06-16 | Warnings | 10028-035-02 10028-035-01 10028-035 10028003502 10028003501 5461ee82-0298-ce22-e063-6294a90a729b 5461ee82-0297-ce22-e063-6294a90a729b |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
