SUMMER FRIDAYS SHADEDROPS BROAD SPECTRUM MINERAL MILK SUNSCREEN SPF 50- titanium dioxide, zinc oxide emulsion

Drug Labeling and Warnings

Drug Details [pdf]

Drug Facts

Drug Facts enclosed

Active ingredients

Titanium Dioxide 5.46%

Zinc Oxide 5.93%

Purpose

Sunscreen

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

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.

Directions

Shake well
Apply liberally 15 minutes before sun exposure
Use a water resistant sunscreen if swimming or sweating
Reapply at least every 2 hours
Children under 6 months of age: Ask a doctor
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 10 AM – 2 PM
Wear long-sleeved shirts, pants, hats, and sunglasses

Other information

Protect this product from excessive heat and direct sun.

Inactive ingredients

WATER/AQUA/EAU, CAPRYLIC/CAPRIC TRIGLYCERIDE, BUTYLOCTYL SALICYLATE, PROPANEDIOL, COCONUT ALKANES, BUTYROSPERMUM PARKII (SHEA) BUTTER, ALUMINA, POLYGLYCERYL-10 DIISOSTEARATE, GLYCERIN, CERAMIDE NP, CHAMOMILLA RECUTITA (MATRICARIA) FLOWER EXTRACT, ETHYLHEXYL METHOXYCRYLENE, ALLANTOIN, POLYHYDROXYSTEARIC ACID, HYDROGENATED LECITHIN, ECTOIN, COCO-CAPRYLATE/CAPRATE, STEARIC ACID, SUCCINOGLYCAN, TOCOPHEROL, ASCORBYL GLUCOSIDE, GLYCINE SOJA (SOYBEAN) OIL, TRIETHOXYCAPRYLYLSILANE, 1,2-HEXANEDIOL, BENZYL ALCOHOL, PHENOXYETHANOL, TOCOPHERYL ACETATE, SILICA, XANTHAN GUM, DISTARCH PHOSPHATE, CAPRYLHYDROXAMIC ACID, DIETHYLHEXYL SYRINGYLIDENEMALONATE, CARAMEL .

Product Labeling

INGREDIENTS AND APPEARANCE

SUMMER FRIDAYS SHADEDROPS BROAD SPECTRUM MINERAL MILK SUNSCREEN SPF 50 
titanium dioxide, zinc oxide emulsion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81678-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	54.6 mg  in 1 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	59.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
CARAMEL (UNII: T9D99G2B1R)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
ECTOIN (UNII: 7GXZ3858RY)
SUCCINOGLYCAN (AGROBACTERIUM TUMEFACIENS) (UNII: YP632MQS35)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
XANTHAN GUM (UNII: TTV12P4NEE)
COCONUT ALKANES (UNII: 1E5KJY107T)
CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
STEARIC ACID (UNII: 4ELV7Z65AP)
ALUMINA (UNII: LMI26O6933)
ALLANTOIN (UNII: 344S277G0Z)
TOCOPHEROL (UNII: R0ZB2556P8)
SHEA BUTTER (UNII: K49155WL9Y)
WATER (UNII: 059QF0KO0R)
CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)
POLYGLYCERYL-10 DIISOSTEARATE (UNII: 84YE9R8P8T)
ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW)
SOYBEAN OIL (UNII: 241ATL177A)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
BENZYL ALCOHOL (UNII: LKG8494WBH)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
CHAMOMILE (UNII: FGL3685T2X)
PROPANEDIOL (UNII: 5965N8W85T)
HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8)
COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
DISTARCH PHOSPHATE, CORN (UNII: JFB4DJZ8BR)
DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
CERAMIDE NP (UNII: 4370DF050B)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81678-001-50	1 in 1 CARTON	05/05/2026
1		50 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
2	NDC: 81678-001-15	1 in 1 CARTON	05/05/2026
2		15 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
3	NDC: 81678-001-05	1 in 1 CARTON	05/05/2026
3		5 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	05/05/2026

Labeler - Summer Friday's LLC (118620216)