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

Menu
Search

LUBRIDERM

Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.

Lubriderm Advanced Therapy Moisturizing Lotion SPF 30


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Purpose

Active Ingredients Purpose
Avobenzone 3% Sunscreen
Homosalate 6% Sunscreen
Octisalate 5% Sunscreen
Oxybenzone 5% Sunscreen
Octocrylene 4% Sunscreen

LUBRIDERM Uses

  • Helps prevent sunburn
  • Higher SPF gives more sunburn protection
  • Provides high protection against sunburn

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 reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Apply liberally before sun exposure and as needed.
  • Children under 6 months of age: ask a doctor.

Other Information

Sun Alert: Limiting sun exposure, wearing protective clothing, and using sunscreens may reduce the risk of skin aging, skin cancer, and other harmful effects of the sun.

Inactive Ingredients

Water, C12-15 Alkyl Benzoate, Hydroxypropyl Starch Phosphate, Cetearyl Alcohol, Glycerin, Distearyldimonium Chloride, Stearyl Alcohol, Ceteareth-20, Fragrance, Linum Usitatissimum (Linseed) Seed Oil, Panthenol, Tocopheryl Acetate, Disodium EDTA, Rosmarinus Officinalis (Rosemary) Leaf Extract, Methylisothiazolinone

Questions?

Call 1-877-543-8477or visit www.lubriderm.com

PRINCIPAL DISPLAY PANEL - 28g Carton

Lubriderm®
dermatologist developed

Advanced
Therapy
LOTION

Moisturizer
with Sunscreen
SPF 30
HYDRATES EXTRA-DRY SKIN
LONG-LASTING UVA/UVB PROTECTION
NON-GREASY

Net Wt. 1 Oz. (28g)

LUBRIDERM

LUBRIDERM

Avobenzone, Homosalate, Octisalate, Oxybenzone and Octocrylene LOTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:58232-0748
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
AVOBENZONE AVOBENZONE 30 mg
HOMOSALATE Homosalate 60 mg
OCTISALATE OCTISALATE 50 mg
OXYBENZONE OXYBENZONE 50 mg
OCTOCRYLENE Octocrylene 35.5 mg

Inactive Ingredients

Ingredient Name Strength
water
ALKYL (C12-15) BENZOATE
CETOSTEARYL ALCOHOL
GLYCERIN
DISTEARYLDIMONIUM CHLORIDE
stearyl alcohol
POLYOXYL 20 CETOSTEARYL ETHER
LINSEED OIL
PANTHENOL
.ALPHA.-TOCOPHEROL ACETATE
EDETATE DISODIUM
ROSEMARY
METHYLISOTHIAZOLINONE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:58232-0748-8 227 in 1 TUBE
2 NDC:58232-0748-6 28 in 1 TUBE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2010-03-30


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.