FDA.reportPublic FDA data

Rain Skincare Mineral Facial Sunscreen

Manufacturer
Rain Africa Innovations (Pty) Ltd
Effective date
2025-01-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 20:43:07

Label at a glance#

ProductRain Skincare Mineral Facial Sunscreen
Active ingredientZINC OXIDE
Label structure8 sections

Indications and uses

Helps prevent sunburn. Helps prevent sunburn

Dosage and administration

Apply a generous amount at least 15 minutes before sun exposure; reapply at least every 2 hours. Use a water resistant sunscreen if swimming or sweating. Apply a generous amount at least 15 minutes before sun exposure; reapply at least every 2 hours.

Storage and handling

Store below 25℃ away from direct sunlight.

Label contents#

Full prescribing information#

Uses:

INDICATIONS & USAGE SECTION

Helps prevent sunburn.

OTC - PURPOSE SECTION

Helps prevent sunburn

Directions:

INSTRUCTIONS FOR USE SECTION

Apply a generous amount at least 15 minutes before sun exposure; reapply at least every 2 hours. Use a water resistant sunscreen if swimming or sweating.

DOSAGE & ADMINISTRATION SECTION

Apply a generous amount at least 15 minutes before sun exposure; reapply at least every 2 hours.

Sun Protection Measures:

OTHER SAFETY INFORMATION

Spending time in the sun increases your risk of skin cancer and early skin ageing. 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. and wear long-sleeved shirts, pants, hats, and sunglasses

Warnings:

WARNINGS SECTION

Keep out of reach of children

For children under 6 months of age: consult a doctor.

If swallowed, get medical help or contact a Poison Control Center right away.

Do not use on damaged or broken skin.

Keep out of eyes. Rinse with water to remove.

Stop use and consult a doctor if rash occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

OTC - STOP USE SECTION

Stop use and consult a doctor if rash occurs.

OTC - ASK DOCTOR SECTION

For children under 6 months of age: consult a doctor.

Stop use and consult a doctor if rash occurs.

STORAGE AND HANDLING SECTION

Store below 25℃ away from direct sunlight.

INACTIVE INGREDIENT SECTION

IngredientsIngredients

Aqua (Water), Zinc Oxide, Caprylic/Capric Triglyceride, Glycerin, Aloe Ferox Leaf Extract, Polyhydroxystearic Acid, Polysorbate 20, Silica, Glyceryl Stearate Citrate, Cetearyl Alcohol, Cetearyl Olivate, Sorbitan Olivate, Benzyl Alcohol, Daucus Carota Sativa (Carrot) Seed Oil, Glyceryl Caprylate, Bentonite, C13-15 Alkane, Coco-Caprylate/Caprate, Squalane, Glyceryl Stearate, Cetyl Alcohol, Levulinic Acid, Sodium Levulinate, Cellulose Gum, Tocopherol, Xanthan Gum, Hydrolyzed Jojoba Esters, Dehydroacetic Acid, Sodium Hyaluronate, Citric Acid, Potassium Sorbate, Sodium Benzoate, Limonene, Linalool

Ingredients

OTC - ACTIVE INGREDIENT SECTION

Aqua (Water), Zinc Oxide, Caprylic/Capric Triglyceride, Glycerin, Aloe Ferox Leaf Extract, Polyhydroxystearic Acid, Polysorbate 20, Silica, Glyceryl Stearate Citrate, Cetearyl Alcohol, Cetearyl Olivate, Sorbitan Olivate, Benzyl Alcohol, Daucus Carota Sativa (Carrot) Seed Oil, Glyceryl Caprylate, Bentonite, C13-15 Alkane, Coco-Caprylate/Caprate, Squalane, Glyceryl Stearate, Cetyl Alcohol, Levulinic Acid, Sodium Levulinate, Cellulose Gum, Tocopherol, Xanthan Gum, Hydrolyzed Jojoba Esters, Dehydroacetic Acid, Sodium Hyaluronate, Citric Acid, Potassium Sorbate, Sodium Benzoate, Limonene, Linalool.

Mineral Facial Sunscreen

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Mineral Facial SunscreenMineral Facial Sunscreen

SPF 40

High Protection

Broad Spectrum UVB/UVA

Products#

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

DailyMed product names page 1 of 1 · 33 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83836-01383836-013-50

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 32 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERYL STEARATE CITRATEWH8T92A065IACT
BENZYL ALCOHOLLKG8494WBHIACT
CARROT SEED OIL595AO13F11IACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
GLYCERYL STEARATE SEFCZ5MH785IIACT
WATER059QF0KO0RIACT
GLYCERYL CAPRYLATETM2TZD4G4AIACT
COCO-CAPRYLATE/CAPRATE8D9H4QU99HIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
HYDROLYZED JOJOBA ESTERS (ACID FORM)UDR641JW8WIACT
DEHYDROACETIC ACID2KAG279R6RIACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
GLYCERINPDC6A3C0OXIACT
SODIUM BENZOATEOJ245FE5EUIACT
CETYL ALCOHOL936JST6JCNIACT
TOCOPHEROLR0ZB2556P8IACT
SILICON DIOXIDEETJ7Z6XBU4IACT
ALOE FEROX LEAF0D145J8EMEIACT
POLYHYDROXYSTEARIC ACID (2300 MW)YXH47AOU0FIACT
ZINC OXIDESOI2LOH54ZACTIB
POLYSORBATE 207T1F30V5YHIACT
SORBITAN OLIVATEMDL271E3GRIACT
CARBOXYMETHYLCELLULOSE SODIUMK679OBS311IACT
C13-15 ALKANE114P5I43UJIACT
HYALURONATE SODIUMYSE9PPT4THIACT
XANTHAN GUMTTV12P4NEEIACT
LEVULINIC ACIDRYX5QG61EIIACT
CETEARYL OLIVATE58B69Q84JOIACT
BENTONITEA3N5ZCN45CIACT
SQUALANEGW89575KF9IACT
SODIUM LEVULINATEVK44E1MQU8IACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT

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
357879c2-7c86-1f8e-e063-6394a90af3c30b4b2f1c-3985-acbe-e063-6294a90ac0952025-05-19WarningsExact identifier
spl set id: 0b4b2f1c-3985-acbe-e063-6294a90ac095

Reported adverse events (FAERS/openFDA)#

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