RYSHI SPF 50 SUNSCREEN- avobenzone 3%, homosalate 15%, octisalate 5%, octocrylene 10% stick

Ryshi SPF 50 Sunscreen by

Drug Labeling and Warnings

Ryshi SPF 50 Sunscreen by is a Otc medication manufactured, distributed, or labeled by Rite Aid, Derma Care Research Labs, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PURPOSE

Sunscreen.

ACTIVE INGREDIENT

Avobenzone 3%, Homosalate 15%, Octisalate 5%, Octocrylene 10%.

INDICATIONS & USAGE

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.

DOSAGE & ADMINISTRATION

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 increased your risk of skin cancer and early skin aging. To decrease this risk, regularly use sunscreen with a Broad Spectrum SPF 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. Children under 6 months: ask a doctor.

INACTIVE INGREDIENT

Aloe Barbadensis Leaf Extract, BHT, Caprylic/Capric Triglyceride, Cetyl Alcohol, C12-15 Alkyl Benzoate, C15-19 Alkane, Ethylhexyl Palmitate, Fragrance, Helianthus Annuus (Sunflower) Seed Oil, Ozokerite, Paraffin, Polyester-8, Theobroma Cacao (Cocoa) Seed Butter, VP/Eicosene Copolymer.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

RYSHI SPF 50 SUNSCREEN 
avobenzone 3%, homosalate 15%, octisalate 5%, octocrylene 10% stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11822-3115
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	3 g  in 100 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	15 g  in 100 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
EICOSYL POVIDONE (UNII: XQQ9MKE2BJ)
CERESIN (UNII: Q1LS2UJO3A)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
C15-19 ALKANE (UNII: CI87N1IM01)
OCTOCRYLENE (UNII: 5A68WGF6WM)	10 g  in 100 g
ETHYLHEXYL PALMITATE (UNII: 2865993309)
PARAFFIN (UNII: I9O0E3H2ZE)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
CETYL ALCOHOL (UNII: 936JST6JCN)
SUNFLOWER OIL (UNII: 3W1JG795YI)
POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED) (UNII: T9296U138P)
COCOA BUTTER (UNII: 512OYT1CRR)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11822-3115-1	43 g in 1 VIAL, PLASTIC; Type 0: Not a Combination Product	07/05/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	07/05/2022

Labeler - Rite Aid (014578892)

Registrant - Derma Care Research Labs, LLC (116817470)

Establishment
Name	Address	ID/FEI	Business Operations
Derma Care Research Labs, LLC		116817470	manufacture(11822-3115)