Neova DNA Damage Control - Active description, usages, side effects, indications, overdosage, supplying and lots more!

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Neova DNA Damage Control - Active

PhotoMedex, Inc.

Neova DNA Damage Control - Active SPF 45 - Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredients

Zinc Oxide 8.0%, Octinoxate 7.5%, Octisalate 3.0%

Purpose

Zinc Oxide - sunscreen, Octinoxate - sunscreen, Octisalate - sunscreen

Neova DNA Damage Control - Active Uses

• Helps prevent sunburn. • Higher SPF gives more
sunburn protection. • Retains SPF after 80 minutes of activity in
the water or perspiring.

Warnings



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 reach of children

If swallowed, contact a Poison Control Center immediately or get medical help right away.

Directions

Apply liberally before sun exposure.
• Reapply as needed or after towel drying, swimming or perspiring. • Children under 6 months of age: ask a doctor.

Other Information

High protection sun 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. Serious side effects associated with use of this product may be reported to this number: 888-966-1010.

Inactive Ingredients

Water (Aqua), Cyclopentasiloxane,
Ethyl Hexyl Isononanoate, Micrococcus Lysate, Plankton
Extract, L-ergothioneine, Dimethicone, Dimethicone/PEG-10/15
Crosspolymer, Lauryl PEG-9 Polymethylsiloxyethyl Dimethicone,
Dimethicone/Vinyl Dimethicone Crosspolymer, Retinyl
Palmitate, Ascorbyl Palmitate (Vitamin C), Sodium Chloride,
Phenoxyethanol, Butylene Glycol, Iodopropynyl Butylcarbamate,
Citric Acid, Sodium Hydroxide.

Image of Box and Label

Neova DNA Damage Control - Active Neova DNA Damage Control - Active

Neova DNA Damage Control - Active

Zinc Oxide, Octinoxate, Octisalate EMULSION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:62362-129
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Zinc Oxide Zinc oxide 8 mL
OCTINOXATE OCTINOXATE 7.5 mL
OCTISALATE OCTISALATE 3 mL

Inactive Ingredients

Ingredient Name Strength
water
CYCLOMETHICONE 5
ETHYLHEXYL ISONONANOATE
Micrococcus Luteus
ERGOTHIONEINE
DIMETHICONE
VITAMIN A PALMITATE
ASCORBYL PALMITATE
SODIUM CHLORIDE
PHENOXYETHANOL
BUTYLENE GLYCOL
IODOPROPYNYL BUTYLCARBAMATE
Citric acid
SODIUM HYDROXIDE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:62362-129-89 89 in 1 TUBE
2 NDC:62362-129-01 1 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2012-01-05


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