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

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Lubriderm Daily

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

Lubriderm® Daily Moisture Lotion™ SPF 15


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Purpose

Active Ingredients Purpose
Avobenzone  (2%) Sunscreen
Octisalate      (4 %) Sunscreen
Octocrylene  (3%) Sunscreen
Oxybenzone (2.2%) Sunscreen

Lubriderm Daily Uses

  • Helps prevent sunburn
  • Higher SPF gives more sunburn protection
  • Provides moderate 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, Glycerin, C12-15 Alkyl Benzoate, Cetyl Alcohol, Glyceryl Stearate, Cetearyl Alcohol, Phenoxyethanol, Ceteareth-20, Stearic Acid, Triethanolamine, Disodium EDTA, Xanthan Gum, Carbomer, Tocopheryl Acetate, Panthenol, Fragrance, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Benzalkonium Chloride, Methylisothiazolinone

Questions?

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

PRINCIPAL DISPLAY PANEL - 400 mL Bottle Label

NEW &
IMPROVED

Lubriderm®
dermatologist developed

Daily
Moisture
LOTION

Moisturizer
with Sunscreen
SPF15

15
SPF
WITH BROAD-SPECTRUM
UVA/UVB PROTECTION

24 CLINICALLY SHOWN TO
MOISTURIZER FOR 24 HOURS

CLEAN, NON-GREASY FEEL

RECOMMENDED
SKIN
CANCER
FOUNDATION

13.5 Fl. Oz. (400 mL)

Lubriderm Daily

Lubriderm Daily

Avobenzone, Octisalate, Octocrylene, and Oxybenzone LOTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:58232-0718
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
AVOBENZONE AVOBENZONE 20 mg
OCTISALATE OCTISALATE 40 mg
OCTOCRYLENE Octocrylene 30 mg
OXYBENZONE OXYBENZONE 22 mg

Inactive Ingredients

Ingredient Name Strength
water
GLYCERIN
ALKYL (C12-15) BENZOATE
CETYL ALCOHOL
GLYCERYL MONOSTEARATE
CETOSTEARYL ALCOHOL
PHENOXYETHANOL
POLYOXYL 20 CETOSTEARYL ETHER
STEARIC ACID
TROLAMINE
EDETATE DISODIUM
XANTHAN GUM
.ALPHA.-TOCOPHEROL ACETATE
PANTHENOL
benzalkonium chloride
METHYLISOTHIAZOLINONE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:58232-0718-1 400 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2010-06-01


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