RITE AID SUNSCREEN- octinoxate, octisalate, oxybenzone lotion

Rite Aid Sunscreen by

Drug Labeling and Warnings

Rite Aid Sunscreen by is a Otc medication manufactured, distributed, or labeled by RITE AID CORPORATION. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Octinoxate   7.5%
Octisalate    5.0%
Oxybenzone 6.0%

Purpose

Sunscreen

Uses

• helps prevent sunburn
• higher SPF gives more sunburn protection
• retains SPF after 80 minutes of activity in the water
  

Warnings

For external use only

When using this product

• keep out of eyes.Rinse with water to remove.

Stop use and ask a doctor if

rash or irritation develops and lasts.

Keep out of the reach of children.

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

Directions

• apply generously and evenly before sun exposure and as needed
  
• Children under 6 months of age:ask a doctor
• reapply after towel drying, swimming or perspiring
  

Other information

• May stain some fabrics
• Sun Alert: Limiting sun exposure, wearing protective clothing, and using sunscreens may reduce the risks of skin aging, skin cancer, and other harmful effects of the sun.
  

Inactive Ingredients

Water, Stearic Acid, Propylene Glycol, Mineral Oil, Triethanolamine, Cetyl Alcohol, Glycol Stearate, VP/Eicosene Copolymer, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Tocopheryl Acetate, Aloe Barbadensis Leaf Juice, Disodium EDTA, Methylparaben, DMDM Hydantoin, Propylparaben.

Principal Display Panel

VALUE SIZE
RITE AID
SUNSCREEN LOTION
SPF 30
UVA/UVB PROTECTION
Very Sweat Resistant
Very Water Resistant
16 FL OZ( 473 mL)

INGREDIENTS AND APPEARANCE

RITE AID SUNSCREEN  
octinoxate, octisalate, oxybenzone lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11822-9014
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	7.5 g  in 100 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	5 g  in 100 g
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y)	OXYBENZONE	6 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
STEARIC ACID (UNII: 4ELV7Z65AP)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
MINERAL OIL (UNII: T5L8T28FGP)
TROLAMINE (UNII: 9O3K93S3TK)
CETYL ALCOHOL (UNII: 936JST6JCN)
GLYCOL STEARATE (UNII: 0324G66D0E)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
EDETATE DISODIUM (UNII: 7FLD91C86K)
METHYLPARABEN (UNII: A2I8C7HI9T)
DMDM HYDANTOIN (UNII: BYR0546TOW)
PROPYLPARABEN (UNII: Z8IX2SC1OH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11822-9014-9	453 g in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	12/05/2012

Labeler - RITE AID CORPORATION (014578892)