WALGREENS SUNSCREEN SPF 15- octinoxate oxybenzone lotion

Kraj: Stany Zjednoczone

Język: angielski

Źródło: NLM (National Library of Medicine)

Składnik aktywny:

Octinoxate 7.5%, Oxybenzone 4.5%

Dostępny od:

WALGREEN CO.

Droga podania:

TOPICAL

Typ recepty:

OTC DRUG

Wskazania:

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

Status autoryzacji:

OTC monograph not final

Charakterystyka produktu

WALGREENS SUNSCREEN SPF 15- OCTINOXATE OXYBENZONE LOTION
WALGREEN CO.
_Disclaimer: Most OTC drugs are not reviewed and approved by FDA,
however they may be marketed if they_
_comply with applicable regulations and policies. FDA has not
evaluated whether this product complies._
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DRUG FACTS
ACTIVE INGREDIENTS
Octinoxate 7.5%
Oxybenzone 4.5%
PURPOS E
Sunscreen
US ES
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 frequently and after towel drying, swimming or perspiring.
INACTIVE INGREDIENTS
Water, Stearic Acid, Sorbitol, Sorbitan Oleate, Glyceryl Stearate SE,
Hydrogenated Vegetable oil
Isopropyl Myristate, Triethanolamine,VP/Eicosene Copolymer, Benzyl
Alcohol, Imadazolidinyl Urea,
Methylparaben, Dimethicone,Carbomer, Fragrance,Simmondsia
Chinensis(Jojoba) Seed Oil,
Propylparaben, Tocopherol, Aloe Barbadensis Leaf Juice, Disodium EDTA.
PRINCIPAL DISPLAY PANEL
Mix and Match $2.99 each
2/$5
Walgreens
SUNSCREEN
LOTION
UVA/UVB
PROTECTION
VERY WATER RESISTANT
SPF
15
3 FL OZ (89 mL)
WALGREENS SUNSCREEN SPF 15
octinoxate oxybenzone lotion
WALGREEN CO.
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:0 36 3-40 0 1
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
O CTINO XATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)
OCTINOXATE
7.5 g in 10 0 g
O XYBENZO NE (UNII: 9 5OOS7VE0 Y) (OXYBENZONE - UNII:9 5OOS7VE0 Y)
OXYBENZONE
4.5 g in 10 0 g
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
WATER (UNII: 0 59 QF0 KO0 R)
STEARIC ACID (UNII: 4ELV7Z6 5AP)
SO RBITO L (UN