OTC - ACTIVE INGREDIENT SECTION
Active Ingredient Purpose
Zinc Oxide20%....Sunscreen
Standard Procedure Silk Mineral SPF 50 Sunscreen Face Lotion
- Manufacturer
- Baxter Laboratories
- Effective date
- 2025-04-28
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 01:00:36
Label at a glance#
ProductSilk Mineral SPF 50 Sunscreen Face
Active ingredientZINC OXIDE
Label structure8 sections
Label contents#
Full prescribing information#
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 product is swallowed, get medical help or contact a poison control center right awa.
INDICATIONS & USAGE SECTION
Stop use and ask a doctor if rash occurs.
WARNINGS SECTION
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 SECTION
Directions
Apply liberally 15 minutes before sun exposure
Reapply at least every 2 hours
INACTIVE INGREDIENT SECTION
Ingredients
Aqua/Water/Eau, Coco-Caprylate/Caprate, Isohexadecane, Caprylic/Capric Triglyceride, Coco-Caprylate, Polyglyceryl-2 Dipolyhydroxystearate, Isoamyl Laurate, Pentylene Glycol, Isododecane, Polyglyceryl-3 Polyricinoleate, Polyglyceryl-3 Diisostearate, Sorbitan Olivate, Magnesium Sulfate, Polyhydroxystearic Acid, Glycerin, Pongamia Pinnata Seed Extract, Terminalia Ferdinandiana Fruit Extract, Isostearic Acid, Disteardimonium Hectorite, Hydroxyacetophenone, Propylene Carbonate
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Standard Procedure
Silk Mineral SPF 50 Sunscreen Face Lotion
1.7 fl oz 50 mL
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70157-026-01 | Silk Mineral SPF 50 Sunscreen Face | 50 mL in 1 BOTTLE | LOTION | 50 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Silk Mineral SPF 50 Sunscreen Face
- Zinc Oxide
- PENTYLENE GLYCOL
- POLYHYDROXYSTEARIC ACID (2300 MW)
- GLYCERIN
- KAKADU PLUM
- WATER
- COCO-CAPRYLATE/CAPRATE
- COCO-CAPRYLATE
- POLYGLYCERYL-3 PENTARICINOLEATE
- CAPRYLIC/CAPRIC TRIGLYCERIDE
- POLYGLYCERYL-3 DIISOSTEARATE
- PROPYLENE CARBONATE
- ISODODECANE
- DISTEARDIMONIUM HECTORITE
- HYDROXYACETOPHENONE
- PONGAMIA PINNATA SEED
- ISOSTEARIC ACID
- ISOAMYL LAURATE
- ISOHEXADECANE
- SORBITAN OLIVATE
- MAGNESIUM SULFATE
- POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 70157-026 | 70157-026-01 |
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 |
|---|---|---|---|---|---|---|
| Silk Mineral SPF 50 Sunscreen Face | ZINC OXIDE | Baxter Laboratories | 33ddaac7-925e-259c-e063-6294a90a120c | 2025-04-28 | Warnings | 70157-026-01 70157-026 70157002601 33ddaac7-925f-259c-e063-6294a90a120c 33ddaac7-925e-259c-e063-6294a90a120c |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.