NU-DERM HEALTHY SKIN PROTECTION description, usages, side effects, indications, overdosage, supplying and lots more!

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NU-DERM HEALTHY SKIN PROTECTION

OMP, INC.

NU-DERM HEALTHY SKIN PROTECTION SPF 35


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredients

Octinoxate, 7.5%, Zinc oxide, 9%

Purpose

Sunscreens

NU-DERM HEALTHY SKIN PROTECTION Uses

  • Helps prevent sunburn.
  • Higher SPF gives more sunburn protection.

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 15 minutes before sun exposure.
  • Children under six months of age: ask a doctor.
  • Reapply as needed or after towel drying, swimming or perspiring.

NU-DERM HEALTHY SKIN PROTECTION Other information

  • Store at controlled room temperature: 15°-30°C (59°-86°F).
  • High sun protection product.
  • 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

butylparaben, cetearyl alcohol, citric acid, C13-14 isoparaffin, diethanolamine cetyl phosphate, disodium edetate, ethylparaben, isobutylparaben, isopropyl palmitate, laureth-7, methylparaben, octyl stearate, phenoxyethanol, polyacrylamide, polyether-1, polysorbate 60, propylparaben, purified water, sodium hydroxide, triethoxycaprylysilane.

Dist. by OMP, Inc., Long Beach, CA 90802

PRINCIPAL DISPLAY PANEL - 90 mL Bottle Label

THE SKIN CANCER FOUNDATION
RECOMMENDED

The Skin Cancer Foundation
recommends this Product as
an effective UV sunscreen

OBAGI
NU-DERM
®

AM

HEALTHY SKIN
PROTECTION
SPF 35

6

BROAD-SPECTRUM
UVA/UVB SUNSCREEN

3 FL.OZ. (90 mL)

NU-DERM HEALTHY SKIN PROTECTION

NU-DERM HEALTHY SKIN PROTECTION

OCTINOXATE and ZINC OXIDE CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:62032-200
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 75 mg
Zinc Oxide Zinc oxide 90 mg

Inactive Ingredients

Ingredient Name Strength
ISOPROPYL PALMITATE
water
ETHYLHEXYL STEARATE
CETOSTEARYL ALCOHOL
POLYSORBATE 60
C13-14 ISOPARAFFIN
METHYLPARABEN
LAURETH-7
PROPYLPARABEN
EDETATE DISODIUM
BUTYLPARABEN
DIETHANOLAMINE CETYL PHOSPHATE
PHENOXYETHANOL
ETHYLPARABEN
isobutylparaben
SODIUM HYDROXIDE
TRIETHOXYCAPRYLYLSILANE
CITRIC ACID MONOHYDRATE

Product Characteristics

Color
WHITE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:62032-200-10 30 in 1 BOTTLE, PLASTIC
2 NDC:62032-200-90 90 in 1 BOTTLE, PLASTIC
3 NDC:62032-200-08 6 in 1 TUBE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2002-01-01


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