LATHER- DAILY DEFENSE MINERAL SPF 50 BODY SUNSCREEN- zinc oxide cream

LATHER- DAILY DEFENSE MINERAL SPF 50 BODY SUNSCREEN by

Drug Labeling and Warnings

LATHER- DAILY DEFENSE MINERAL SPF 50 BODY SUNSCREEN by is a Otc medication manufactured, distributed, or labeled by Lather, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients

Zinc Oxide 21%

PURPOSE

Purpose Sunscreen

INDICATIONS & USAGE

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

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.

Stop use and ask a doctor if rash occurs

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

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

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

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

Lather

broad spectrum SPF 50

water resistant (80 minutes)

FRAGRANCE-FREE

for adults and children

3 fl oz / 88 mL

INGREDIENTS AND APPEARANCE

LATHER- DAILY DEFENSE MINERAL SPF 50 BODY SUNSCREEN 
zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77394-203
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	21 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
OLEA EUROPAEA (OLIVE) LEAF (UNII: MJ95C3OH47)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
ASCORBIC ACID (UNII: PQ6CK8PD0R)
MICA (UNII: V8A1AW0880)
CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
TOCOPHEROL (UNII: R0ZB2556P8)
CETEARYL ALCOHOL (UNII: 2DMT128M1S)
PROPANEDIOL (UNII: 5965N8W85T)
GLYCERIN (UNII: PDC6A3C0OX)
XANTHAN GUM (UNII: TTV12P4NEE)
CENTELLA ASIATICA (UNII: 7M867G6T1U)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
BUTYROSPERMUM PARKII (SHEA) BUTTER (UNII: K49155WL9Y)
GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
SILICA (UNII: ETJ7Z6XBU4)
CITRIC ACID (UNII: 2968PHW8QP)
SODIUM PHYTATE (UNII: 88496G1ERL)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ASCORBYL PALMITATE (UNII: QN83US2B0N)
CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)
EQUISETUM ARVENSE BRANCH (UNII: 1L0VKZ185E)
SORBITAN OLIVATE (UNII: MDL271E3GR)
CETEARYL OLIVATE (UNII: 58B69Q84JO)
HORSE CHESTNUT (UNII: 3C18L6RJAZ)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77394-203-03	88 mL in 1 TUBE; Type 0: Not a Combination Product	05/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	05/01/2025

Labeler - Lather, Inc. (100666606)