FDA.reportPublic FDA data

LATHER- DAILY DEFENSE MINERAL SPF 50 BODY SUNSCREEN

Manufacturer
Lather, Inc.
Effective date
2025-10-15
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:39:06

Label at a glance#

ProductLATHER- DAILY DEFENSE MINERAL SPF 50 BODY SUNSCREEN
Active ingredientZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients

Zinc Oxide 21%

OTC - PURPOSE SECTION

Purpose Sunscreen

INDICATIONS & USAGE 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

WARNINGS SECTION

Warnings For external use only

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin

OTC - WHEN USING SECTION

When using this product keep out of eyes. Rinse with water to remove.

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

SPL UNCLASSIFIED SECTION

Other information: protect this product from excessive heat and direct

DOSAGE & ADMINISTRATION SECTION

Directions: Apply liberally 15 minutes before sun exposure. reapply: after 80 minutes of swimming or sweating. immediately after towel drying. at least every 2 hours. 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 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-sleeve shirts, pants, hats, and sunglasses, children under 6 months of age: ask a doctor

INACTIVE INGREDIENT SECTION

Inactive ingredients: Water (Aqua), Coco Caprylate/Caprate, Cetearyl Alcohol, Propanediol, Stearyl Alcohol, Polyhydroxystearic Acid, Mica, Butyrospermum Parkii (Shea) Butter, Cetearyl Olivate, Sorbitan Olivate, Caprylhydroxamic Acid, Glyceryl Caprylate, Glycerin, Xanthan Gum, Equisetum Arvense (Horsetail) Extract, Rosmarinus Officinalis (Rosemary) Extract, Centella Asiatica (Gotu Kola) Extract, Aesculus Hippocastanum (Horse Chestnut) Extract, Camellia Sinensis (Green Tea) Extract, Olea Europaea (Olive) Leaf Extract, Tocopheryl Acetate, Potassium Sorbate, Sodium Phytate, Silica, Triethoxycaprylylsilane, Ascorbyl Palmitate, Caprylic/Capric Triglyceride, Ascorbic Acid, Tocopherol, Citric Acid

Lather - daily defense mineral SPF 50 - 3 fl oz / 88 mL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

daily defense mineral SPF 50
body sunscreen with UVA/UVB protection

Lather Lather - daily defense mineral SPF 50 - 3 fl oz / 88 mLLather - daily defense mineral SPF 50 - 3 fl oz / 88 mL

broad spectrum SPF 50

water resistant (80 minutes)

FRAGRANCE-FREE

for adults and children

3 fl oz / 88 mL

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130836583007361GTIN-13: 0836583007361
EAN-13: 0836583007361
GTIN-12: 836583007361
UPC-A: 836583007361
GTIN storage (14 digits): 00836583007361		daily-defense-minera-SPF-50-body-3oz_OL_FDA.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77394-203-03LATHER- DAILY DEFENSE MINERAL SPF 50 BODY SUNSCREEN88 mL in 1 TUBECREAM882

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
77394-20377394-203-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 29 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
STEARYL ALCOHOL2KR89I4H1YIACT
OLEA EUROPAEA (OLIVE) LEAFMJ95C3OH47IACT
POTASSIUM SORBATE1VPU26JZZ4IACT
ASCORBIC ACIDPQ6CK8PD0RIACT
MICAV8A1AW0880IACT
CAPRYLHYDROXAMIC ACIDUPY805K99WIACT
TOCOPHEROLR0ZB2556P8IACT
GLYCERINPDC6A3C0OXIACT
ZINC OXIDESOI2LOH54ZACTIB
CETEARYL ALCOHOL2DMT128M1SIACT
PROPANEDIOL5965N8W85TIACT
XANTHAN GUMTTV12P4NEEIACT
CENTELLA ASIATICA7M867G6T1UIACT
GLYCERYL CAPRYLATETM2TZD4G4AIACT
POLYHYDROXYSTEARIC ACID (2300 MW)YXH47AOU0FIACT
COCO-CAPRYLATE/CAPRATE8D9H4QU99HIACT
BUTYROSPERMUM PARKII (SHEA) BUTTERK49155WL9YIACT
SILICAETJ7Z6XBU4IACT
CITRIC ACID2968PHW8QPIACT
TRIETHOXYCAPRYLYLSILANELDC331P08EIACT
SODIUM PHYTATE88496G1ERLIACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
ASCORBYL PALMITATEQN83US2B0NIACT
CAPRYLIC/CAPRIC TRIGLYCERIDEC9H2L21V7UIACT
EQUISETUM ARVENSE BRANCH1L0VKZ185EIACT
SORBITAN OLIVATEMDL271E3GRIACT
CETEARYL OLIVATE58B69Q84JOIACT
HORSE CHESTNUT3C18L6RJAZIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12025-03-27full-release2026-06-01 01:00:03

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
LATHER- DAILY DEFENSE MINERAL SPF 50 BODY SUNSCREENZINC OXIDELather, Inc.3158a2d7-0db5-f5bf-e063-6294a90a31262025-10-15WarningsExact identifier
ndc (package): 77394-203-03
ndc (product): 77394-203
ndc11 (package): 77394020303
spl id: 4135b305-af4e-c673-e063-6394a90aae20
spl set id: 3158a2d7-0db5-f5bf-e063-6294a90a3126

Reported adverse events (FAERS/openFDA)#

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