PETER ISLAND SUNSCREEN SPF 50- homosalate, oxybenzone, octisalate, avobenzone, octocrylene lotion

Land: USA

Språk: engelsk

Kilde: NLM (National Library of Medicine)

Tilgjengelig fra:

AMWAY CORP.

Administreringsrute:

TOPICAL

Resept typen:

OTC DRUG

Autorisasjon status:

OTC monograph not final

Preparatomtale

PETER ISLAND SUNSCREEN SPF 50- HOMOSALATE, OXYBENZONE, OCTISALATE,
AVOBENZONE,
OCTOCRYLENE LOTION
AMWAY CORP.
_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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ACTIVE INGREDIENTS
Homosalate 13.0%
Octocrylene 7.0%
Octisalate 5.0%
Oxybenzone 4.0%
Avobenzone 3.0%
WARNING
FOR EXTERNAL USE ONLY.
Avoid contact with eyes. Rinse with water if contact occurs.
Discontinue use if signs of rash or irritation develop.
For use on children under the age of 6 months consult a physician.
Keep out of reach of children.
DIRECTIONS
Apply generously and evenly 30 minutes before sun exposure. Reapply
frequently and after swimming,
excessive perspiration and towel drying.
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.
This oil tree formula provides broad spectrum UVA/UVB protection from
the sun's damaging rays. It is
PABA free, vitamin enriched and very water resistant.
PRINCIPAL DISPLAY PANEL
PETER ISLAND
Sunscreen lotion
spf 50
Photostable
Broad Spectrum
UVA/UVB Protection
Very Water Resistant
8 FL.OZ. (237 mL)
INACTIVE INGREDIENTS
Water, Sorbitol, Stearic Acid,Triethanolamine, Aluminum Starch
Octenylsuccinate, Benzyl
Alcohol,Sorbitan Isostearate, VP/Eicosene Copolymer, Dimethicone,
Polyglyceryl-3 Distearate,
Carbomer, Tocopherol, Disodium EDTA, Methylparaben, Propylparaben,
Fragrance.
PETER ISLAND SUNSCREEN SPF 50
homosalate, oxybenzone, octisalate, avobenzone, octocrylene lotion
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:50 39 0 -70 2
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
HO MO SALATE (UNII: V0 6 SV4M9 5S) (HOMOSALATE - UNII:V0 6 SV4M9 5S)
HOMOSALATE
13 g in 10 0 g
O XYBENZO NE (UNII: 9 5OOS7VE0 Y) (OXYB