Kroger 959.001/959AB Ultra Sunscreen Spray SPF 30

sunscreen by

Drug Labeling and Warnings

sunscreen by is a Otc medication manufactured, distributed, or labeled by Kroger, Vi-Jon, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SUNSCREEN- avobenzone, homosalate, octisalate, octocrylene spray 
The Kroger Co.

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Kroger 959.001/959AB
Ultra Sunscreen Spray SPF 30

Claims

Kroger Sunscreen Spray SPF 30 provides quick and easy coverage with broad-spectrum protection.  Its clear, specially formulated spray goes on at any angle. Water-resistant formula provides protection in and out of water for up to 80 minutes.

Active ingredients

Avobenzone 3%

Homosalate 10%

Octisalate 5%

Octocrylene 8%

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

Flammable:

Keep away from fire or flame.

• after application, wait until product dries before approacing a souce 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 Conrol 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 spray directly into face. Spray on hands then apply to face.
■ do not apply in windy conditions
■ 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 in the container from excessive heat and direct sun

Inactive ingredients

alcohol denat., acrylates/octylacrylamide copolymer, glycerin, triethanolamine, tocopherol, fragrance, butyloctyl salicylate

ADVERSE REACTION

May stain or damage some fabrics or surfaces

DISTRIBUTED BY THE KROGER CO., CINCINNATI, OHIO 45202

*COPPERTONE ®AND COPPERTONE ULTRA GUARD ®ARE REGISTERED TRADEMARKS OF BEIERSDORF AG.

BEIERSDORF IS NOT AFFILATED WITH THE KROGER CO. OR THIS PRODUCT.

**Oxybenzone & Octinoxate free

QUALITY GUARANTEE

800-632-6900 

www.kroger.com

Principal display panel

compare to COPPERTONE ®ULTRA GUARD ®*see back panel

Kroger ®

SUNSCREEN SPRAY

BROAD SPECTRUM SPF 30

UVA/UVB protection

hypoallergenic

continuous spray

water resistant (80 minutes)

sweat resistant

SPF 30

REEF FRIENDLY**

NET WT 5.5 OZ (156 g)

SUNSCREEN 
avobenzone, homosalate, octisalate, octocrylene spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 30142-075
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
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	80 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)
GLYCERIN (UNII: PDC6A3C0OX)
TROLAMINE (UNII: 9O3K93S3TK)
TOCOPHEROL (UNII: R0ZB2556P8)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 30142-075-14	156 g in 1 CAN; Type 0: Not a Combination Product	01/18/2021	03/06/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	01/18/2021	03/13/2026

Labeler - The Kroger Co. (006999528)

Registrant - Nice-Pak Products, LLC (119091520)

Establishment
Name	Address	ID/FEI	Business Operations
Nice-Pak Products, LLC		119091514	manufacture(30142-075)

Revised: 3/2026

Document Id: 4ce8d76f-c12b-678b-e063-6294a90a3d42

34390-5

Set id: 95871f35-3413-43c2-9745-7913b84ef215

Version: 10

Effective Time: 20260313