SOLBAR THIRTY- sunscreen gel

SOLBAR THIRTY by

Drug Labeling and Warnings

SOLBAR THIRTY by is a Otc medication manufactured, distributed, or labeled by Person and Covey. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Homosalate 12.0%

Octinoxate 7.5%

Oxybenzone 6.0%

Avobenzone 3.0%

Octocrylene 1.5%

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

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: Ask a doctor.

Inactive Ingredients

SD Alcohol, Isobutyl Stearate, Cyclomethicone, PVP/Eicosene Copolymer, Dimethicone, Hydroxypropylcellulose, Acrylates/Octylacrylamide Copolymer.

Other Information

Store away from excessive heat or cold.

Questions?

Please call 1 (800) 423-2341

Company Information

Person & Covey, Inc. Glendale, California 91201, U.S.A. MADE IN USA personandcovey.com

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SOLBAR THIRTY 
sunscreen gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0096-0689
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y)	OXYBENZONE	60 mg  in 1 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	15 mg  in 1 g
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	30 mg  in 1 g
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	75 mg  in 1 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	120 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
HYDROXYPROPYLCELLULOSE (UNII: 9XZ8H6N6OH)
ACRYLATES/OCTYLACRYLAMIDE COPOLYMER (75000 MW) (UNII: JU3XHR8VWK)
ALCOHOL (UNII: 3K9958V90M)
ISOBUTYL STEARATE (UNII: V8DPR6HNX3)
DIMETHICONE (UNII: 92RU3N3Y1O)
EICOSYL POVIDONE (UNII: XQQ9MKE2BJ)
CYCLOMETHICONE (UNII: NMQ347994Z)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0096-0689-03	90 g in 1 TUBE; Type 0: Not a Combination Product	01/22/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	01/22/2026

Labeler - Person and Covey (008482473)

Registrant - Person and Covey (008482473)

Establishment
Name	Address	ID/FEI	Business Operations
Person and Covey		008482473	manufacture(0096-0689)