PCA SKIN Body Hydrator description, usages, side effects, indications, overdosage, supplying and lots more!

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PCA SKIN Body Hydrator

Physicians Care Alliance, LLC DBA PCA SKIN

Perfecting Protection SPF 30




FULL PRESCRIBING INFORMATION

Active ingredient

DRUG FACTS

_________________________________

Active Ingredient:         Purpose:

Zinc Oxide(9.8%)         Sunscreen (UVA UVB)

Octinoxate(7.5%)         Sunscreen (UVB)

Uses

Uses:  Provides high protection against sunburn.

Warnings: For external use only. Keep out of eyes. Rinse with water to remove.  Stop use and consult a physician ifskin rash and irritation develops and lasts.

Directions:For use by adults and children six months and older.  apply liberally to exposed areas at least 30 minutes prior to sun exposure.  Reapply every two hours or as needed after swimming or perspiring.  Consult a physician prior to use on children under six months of age.

Other Information:  Sun Alert. Limiting sun exposure, wearing protecting clothing and using sunscreens may reduce the risks of skin aging, skin cancer and other harmful effects of the sun.

Inactive Ingredients:Water/Aqua/Eau, Ethylhexyl Palmitate, GLycerin, Cyclopentasiloxane, Isononyl Isononanoate, Cetearyl Alcohol, SD Alcohol 40-B, Polyacrylate-13, Dimethicone, Tocopheryl Acetate, Triethoxycaprylylsilane, Lactic Acid, Kojic Acid, Butylene Glycol, Morus Alba Root Extract, Arctostaphylos, Uva Ursi Leaf Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Caffeine, Silybum Marianum Extract, Arginine, Microcrystalline Cellulose, C20-22 Allcohols, Polyisobutene, Cetearyl Glucoside, Caprylyl Glycol, Cellulose Gum, Aloe Barbadensis Leaf Juice, Sodium PCA, Sodium Hyaluronate, Magnesium Ascorbyl Phosphate, Tetrasodium EDTA, Cirtus Grandis (Grapefruit) Peel oil, Ethylhexylglycerin, Phenoxyethanol.


PCA SKIN Body Hydrator

Perfecting Protection SPF 30

Broad Spectrum UVA/UVB Sunscreen

PCA skin

Net wt 7oz/198.4g

PCA SKIN Body Hydrator

Zinc Oxide and Octinoxate LOTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:68726-167
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Zinc Oxide Zinc oxide 9.8 g
OCTINOXATE OCTINOXATE 7.5 g

Inactive Ingredients

Ingredient Name Strength
water
GLYCERIN
CYCLOMETHICONE 5
1,3-BUTYLENE GLYCOL
CETOSTEARYL ALCOHOL
CAFFEINE
POLYSORBATE 20
cellulose, microcrystalline
CARBOXYMETHYLCELLULOSE SODIUM
Aloe Vera Leaf
DIMETHICONE
.ALPHA.-TOCOPHEROL ACETATE, D-
VITAMIN A PALMITATE
GLYCYRRHIZA GLABRA
MORUS ALBA ROOT BARK
LACTIC ACID
ARGININE
PHENOXYETHANOL
CAPRYLYL GLYCOL
ETHYLHEXYLGLYCERIN
Hexylene Glycol
CITRUS PARADISI SEED
ALCOHOL
MILK THISTLE
KOJIC ACID
SODIUM HYDROXIDE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:68726-167-01 198.4 in 1 BOTTLE
2 NDC:68726-167-02 48 in 1 BOTTLE
3 NDC:68726-167-03 9 in 1 TUBE
4 NDC:68726-167-04 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2010-10-01


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