Nu Skin description, usages, side effects, indications, overdosage, supplying and lots more!

Nu Skin

NSE Products, Inc.

  • Description
  • Clinical Pharmacology
  • Indications & Usage
  • Contraindications
  • Warnings
  • Precautions
  • Side Effects
  • Overdosage
  • Dosage & Administration
  • How Supplied
  • Patient Counseling Information
  • Supplemental Patient Material
  • Boxed Warning
  • Patient Package Insert
NU SKIN moisture restore day PROTECTIVE LOTION SPF 15

FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredients

Octinoxate (7.5%), Zinc Oxide (3.8%).

Warning

Keep out of eyes. If rash or irritation develops and persists, discontinue use and consult a physician.

Directions

Using fingertips, apply generously to clean face and neck in an upward, outward motion. Use every morning before makeup application.

Inactive Ingredients

Water (Aqua), Octyldodecyl Neopentanoate, Glycerin, Cetyl Alcohol, Cyclopentasiloxane, Glyceryl Stearate, Limnanthes Alba (Meadowfoam) Seed Oil, PEG-75 Stearate, Dimethicone, Dunaliella Salina Extract,Colorless Carotenoid Butyrospermum Parkii (Shea Butter) Extract, Oenothera Biennis (Evening Primrose) Oil, Tocopheryl Acetate, Calendula Officinalis Flower Extract, Anthemis Nobilis Flower Extract, Tilia Cordata Flower Extract, Centaurea Cyanus Flower Extract, Chamomilla Recutita (Matricaria) Flower Extract, Hypericum Perforatum Flower/Leaf/Stem Extract, Allantoin, Butylene Glycol, Polyacrylate-13, Polyisobutene, Polysorbate 20, Steareth-20, Myristyl Myristate, Polydecene, Ceteth-20, Triethoxycaprylylsilane, Castor Oil Phosphate, Xanthan Gum, Tetrasodium EDTA, Fragrance (Parfum), Phenoxyethanol, Chlorphenesin, Methylparaben, Propylparaben, Benzoic Acid.

Questions?

1-888-742-7626

PRINCIPAL DISPLAY PANEL - 50 ml Carton

NU SKIN

moisture restore
day

PROTECTIVE LOTION
SPF 15

NORMAL
TO DRY SKIN

50 ml e (1.7 fl. oz.)

PRINCIPAL DISPLAY PANEL - 50 ml Carton

Nu Skin

Octinoxate and Titanium Dioxide LOTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:62839-2728
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 75 g
titanium dioxide 38 g

Inactive Ingredients

Ingredient Name Strength
water
OCTYLDODECYL NEOPENTANOATE
GLYCERIN
CETYL ALCOHOL
CYCLOMETHICONE 5
GLYCERYL MONOSTEARATE
MEADOWFOAM SEED OIL
peg-75 stearate
DIMETHICONE
SHEANUT OIL
DUNALIELLA SALINA
EVENING PRIMROSE OIL
CALENDULA OFFICINALIS FLOWER
CHAMAEMELUM NOBILE FLOWER
TILIA CORDATA FLOWER
Centaurea Cyanus Flower
CHAMOMILE
St. John's Wort
ALLANTOIN
BUTYLENE GLYCOL
POLYSORBATE 20
Steareth-20
MYRISTYL MYRISTATE
CETETH-20
TRIETHOXYCAPRYLYLSILANE
XANTHAN GUM
EDETATE SODIUM
PHENOXYETHANOL
CHLORPHENESIN
METHYLPARABEN
PROPYLPARABEN
BENZOIC ACID

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 50 in 1 BOTTLE, PUMP
2 NDC:62839-2728-1 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2001-06-10


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Be sure to consult your doctor before taking any medication!
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