BRUSH ON BLOCK SPF 50 MINERAL- zinc oxide spray

BRUSH ON BLOCK SPF 50 MINERAL by

Drug Labeling and Warnings

BRUSH ON BLOCK SPF 50 MINERAL by is a Otc medication manufactured, distributed, or labeled by SPF Ventures, LLC, PURE SOURCE. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

ZINC OXIDE 15%

Purpose

Sunscreen

Uses

• Helps prevent sunburn
• Higher SPF gives more sunburn protection
• Retains SPF after 80 minutes of swimming or sweating
• If used as directed with other sun protection measure (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.

Warnings

For external use only.

Do not use

Do not use on damaged or broken skin.

When using this product

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

Do not puncture or incinerate. Contents under pressure. Do not store it at temperatures above 120F.

Stop use and ask a doctor

Stop use and ask a doctor if rash or irritation develops and lasts.

Keep out of reach of children

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

If pregnant or breast-feeding

If pregnant or breast-feeding, ask a health professional before use.

Directions

• Apply liberally 15 minutes before sun exposure and as needed;
• Children under 6 months of age: ask a doctor
• Reapply: After 80 minutes of swimming or sweating; Immediately after towel drying; At least every 2 hours; Do not spray directly on face. Spray into hands and apply to face; Use in well-ventilated areas;

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 value of 15 or higher and other sun protection measures including: Limit time in the sun, especially from 10am-2pm; Wear long-sleeved shirts, pants, hats and sunglasses;

Inactive ingredients

ALLANTOIN

ALOE BARBADENSIS LEAF JUICE

BRASSICA OLERACEA ITALICA (BROCCOLI) EXTRACT

BUTYLOCTYL SALICYLATE

C13-16 ISOALKANE

CAMELLIA SINENSIS LEAF EXTRACT

CAPRYLIC/CAPRIC TRIGLYCERIDE

CARTHAMUS TINCTORIOUS (SAFFLOWER) SEED OIL

CITRIC ACID

DECYL GLUCOSIDE

DODECANE

GLYCERIN

GLYCERYL STEARATE CITRATE

GLYCERYL STEARATE SE

HEPTYL UNDECYLENATE

LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE

NIACINAMIDE

PERSEA GRATISSIMA (AVOCADO) OIL

POLYHYDROXYSTEARIC ACID

PROPANEDIOL

SORBITAN STEARATE

TOCOPHERYL ACETATE

TRIDECYL SALICYLATE

WATER (AQUA)

XANTHAN GUM

Other Information

Protect the product in this container from excessive heat and direct sun.

label

INGREDIENTS AND APPEARANCE

BRUSH ON BLOCK SPF 50 MINERAL 
zinc oxide spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58274-026
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	15 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE BARBADENSIS LEAF (UNII: ZY81Z83H0X)
C13-16 ISOPARAFFIN (UNII: LED42LZG6O)
CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)
CITRIC ACID (UNII: 2968PHW8QP)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
DODECANE (UNII: 11A386X1QH)
GLYCERIN (UNII: PDC6A3C0OX)
HEPTYL UNDECYLENATE (UNII: W77QUB6GXO)
NIACINAMIDE (UNII: 25X51I8RD4)
AVOCADO OIL (UNII: 6VNO72PFC1)
SORBITAN STEARATE (UNII: NVZ4I0H58X)
TRIDECYL SALICYLATE (UNII: AZQ08K38Z1)
XANTHAN GUM (UNII: TTV12P4NEE)
LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458)
ALLANTOIN (UNII: 344S277G0Z)
CARTHAMUS TINCTORIUS (SAFFLOWER) SEED OIL (UNII: 65UEH262IS)
CAMELLIA SINENSIS LEAF (UNII: W2ZU1RY8B0)
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
PROPANEDIOL (UNII: 5965N8W85T)
WATER (UNII: 059QF0KO0R)
GLYCERYL STEARATE CITRATE (UNII: WH8T92A065)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
BROCCOLI SPROUT (UNII: 128UH9LOAE)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58274-026-01	177 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	02/27/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	02/27/2025

Labeler - SPF Ventures, LLC (055483891)

Establishment
Name	Address	ID/FEI	Business Operations
PURE SOURCE		080354456	manufacture(58274-026)