Solar Plex 940.000/940AA Ultra Sunscreen Lotion SPF 50

Ultra Sunscreen SPF 50 by

Drug Labeling and Warnings

Ultra Sunscreen SPF 50 by is a Otc medication manufactured, distributed, or labeled by Consumer Product Partners, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ULTRA SUNSCREEN SPF 50- avobenzone, homosalate, octisalate, octocrylene lotion 
Consumer Product Partners, LLC

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Solar Plex 940.000/940AA
Ultra Sunscreen Lotion SPF 50

Active Ingredients

Avobenzone 3%

Homosalate 10%

Octisalate 4.5%

Octocrylene 8%

Purpose

Sunscreen

Uses

• helps prevent sunburn
• if used as directed with other sun protections measures (see Directions), decreases the rist 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 {and evenly} 15 minutes before sun exposure
• apply to all skin exposed to the sun
• 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

water, glycerin, aluminum starch octenylsuccinate, styrene/acrylates copolymer, polyester-7, silica, chlorphenesin, arachidyl alcohol, beeswax, neopentyl glycol diheptanoate, acrylates/C10-30 alkyl acrylate crosspolymer, behenyl alcohol, tocopherol, arachidyl glucoside, glyceryl stearate, PEG-100 stearate, potassium hydroxide, fragrance, benzyl alcohol, disodium EDTA

Disclaimer

May stain or damage some fabrics or surfaces

*This product is not manufactured or distributed by Bayer, distributor of Coppertone Ultra Guard Sunscreen Lotion Broad Spectrum SPF 50.

Adverse reaction

Manufactured by: Vi-Jon, LLC

8515 Page Ave. St. Louis, MO 63114

Principal Panel Display

SPF 50

0869-0940-34

Solar Plex

Ultra Sunscreen Lotion

Broad Spectrum SPF 50

Water Resistant (80 minutes)

Hypoallergenic

Dermatologist tested

Compare to Coppertone sunscreen Lotion Ultra Guard**

8 FL OZ (236 mL)

ULTRA SUNSCREEN SPF 50 
avobenzone, homosalate, octisalate, octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11344-940
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 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	100 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	45 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	80 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
STYRENE (UNII: 44LJ2U959V)
STYRENE/ACRYLAMIDE COPOLYMER (500000 MW) (UNII: 5Z4DPO246A)
POLYESTER-7 (UNII: 0841698D2F)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
CHLORPHENESIN (UNII: I670DAL4SZ)
ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)
YELLOW WAX (UNII: 2ZA36H0S2V)
NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
DOCOSANOL (UNII: 9G1OE216XY)
TOCOPHEROL (UNII: R0ZB2556P8)
ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
PEG-100 STEARATE (UNII: YD01N1999R)
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
BENZYL ALCOHOL (UNII: LKG8494WBH)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11344-940-34	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/22/2022	03/08/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	07/22/2022	03/08/2025

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(11344-940)

Revised: 6/2025

Document Id: 3729edf7-492f-6d29-e063-6294a90a6120

34390-5

Set id: 40757fa0-e347-4eea-9c3c-f1a1aac217d6

Version: 3

Effective Time: 20250609