Wild Tropics D48AA/D48.000 Sunscreen Spray SPF30

Sunscreen SPF 30 by

Drug Labeling and Warnings

Sunscreen SPF 30 by is a Otc medication manufactured, distributed, or labeled by Consumer Product Partners, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SUNSCREEN SPF 30- avobenzone, homosalate, octisalate spray 
Consumer Product Partners, LLC

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Wild Tropics D48AA/D48.000
Sunscreen Spray SPF30

Active ingredients

Avobenzone 3%

Homosalate 10%

Octisalate 5%

Purpose

Sunscreen

Uses

• helps prevent sunburn
• if used as directed with other sun protection measures (see Directions), decreases the rish of skin cancer and early skin aging caused by the sun

Warnings

For external use only

• Flammable:Keep away from fire or flame.
• after application, wait until product dries before approaching a source of heat or flame, or before smoking

Do not use

• on damaged or broken skin

When using this product

• keep out of eyes.  Rinse with water to remove
• contents under pressure. Do not puncture or incinerate. Do not store at temperature above 120ºF.

Stop use and ask a doctor if

• rash occurs

Keep out of reach of children

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

Directions

• spray liberally and spread evenly by hand 15 minutes before sun exposure
• apply to all skin exposed to the sun 
• hold container 4 to 6 inches from the skin to apply
• do not apply in windy conditiona
• use in a well-ventilated area and avoid inhalation
•  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 value 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-sleeved shirts, pants, hats and sunglasses
• children under 6 months of age: Ask a doctor

Other information

• protect the product from excessive heat and direct sun

Inactive ingredients

alcohol denat., diethylhexyl 2,6-naphthalate, acrylates/octylacrylamide copolymer, diisopropyl adipate, neopentyl glycol diheptanoate, butyloctyl salicylate, fragrance, tocopheryl acetate

Disclaimer

May stain or damage some fabrics or surfaces

*This product is not manufactured or distributed by Sun Bum LLC, distributor of Sun Bum ®Premium Moisturizing Sunscreen Spray Broad Spectrum SPF 30.

Adverse reaction

Manufactured by: Vi-Jon, LLC

One Swan Drive

Smyrna, TN 37167

Principal Display Panel

wild tropics ™

SUNSCREEN SPRAY

BROAD SPECTRUM SPF 30

HYPOALLERGENIC

DERMATOLOGIST TESTED

WATER RESISTANT (80 MINUTES)

FRESH BANANA SCENT

Compare to Sun Bum ®Premium Moisturizing Sunscreen Spray*

SPF 30

NET WT 5.5 OZ (156 g)

SUNSCREEN SPF 30 
avobenzone, homosalate, octisalate spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11344-048
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	30 mg  in 1 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	100 mg  in 1 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	50 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
DIETHYLHEXYL 2,6-NAPHTHALATE (UNII: I0DQJ7YGXM)
ACRYLATE/ISOBUTYL METHACRYLATE/N-TERT-OCTYLACRYLAMIDE COPOLYMER (40000 MW) (UNII: 7LL6SY9YFV)
DIISOPROPYL ADIPATE (UNII: P7E6YFV72X)
NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11344-048-14	156 g in 1 CAN; Type 0: Not a Combination Product	03/01/2024	07/16/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	03/01/2024	07/16/2025

Labeler - Consumer Product Partners, LLC (119091520)

Registrant - Consumer Product Partners, LLC (119091520)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091514	manufacture(11344-048)

Revised: 7/2025

Document Id: 3a11932a-c191-15a8-e063-6394a90a5f1a

34390-5

Set id: 3ebff656-0238-42c8-8886-5bebd37b62ef

Version: 2

Effective Time: 20250716