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

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EQUALINE

SUPERVALU INC.
APOLLO HEALTH AND BEAUTY CARE

DRUG FACTS


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENTS

OCTISALATE 5.0%, AVOBENZONE 3.0%, HOMOSALATE 3.0%, OCTOCRYLENE 2.6%

PURPOSE

SUNSCREEN

USE(S)

HELPS PREVENT SUNBURN. IF USED AS DIRECTED WITH OTHER SUN PROTECTION MEASURES (SEE DIRECTIONS), DECREASES THE RISK OF SKIN CANCER AND EARLY SKIN AGING CAUSED BY THE SUN.

WARNINGS

FOR EXTERNAL USE ONLY.

DO NOT USE

ON DAMAGED OR BROKEN SKIN.

WHEN USING THIS PRODUCT

KEEP OUT OF EYES. RINSE WITH WATER TO REMOVE.

STOP USING THIS PRODUCT AND ASK A DOCTOR IF

RASH OCCURS.

KEEP OUT OF REACH OF CHILDREN

IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.

DIRECTIONS

APPLY LIBERALLY 15 MINUTES BEFORE SUN EXPOSURE. USE A WATER RESISTANT SUNSCREEN IF SWIMMING OR SWEATING. REAPPLY AT LEAST EVERY 2 HOURS. CHILDREN UNDER 6 MONTHS: ASK A DOCTOR.

SUN PROTECTION MEASURES. SPENDING TIME IN THE SUN INCREASES YOUR RISK OF SKIN CANACER AND EARLY SKIN AGING. TO DECREASE THIS RISK, REGULARLY USE A SUNSCREEN WITH A BROAD SPECTRUM SPF VALUE OF 15 OR HIGHER AND OTHER SUN PROTECTION MEASURES INCLUDING: LIMIT TIME IN THE SUN, ESPECIALLY FROM 10 A.M. - 2 P.M., WEAR LONG-SLEEVED SHIRTS, PANTS, HATS, AND SUNGLASSES.

OTHER INFORMATION

PROTECT THIS PRODUCT FROM EXCESSIVE HEAT AND DIRECT SUN.

INACTIVE INGREDIENTS:

ASCORBIC ACID, BEHENYL ALCOHOL, BENZYL ALCOHOL, CETEARYL ALCOHOL, CETEARYL GLUCOSIDE, CETYL ALCOHOL, DIMETHICONE, DIMETHICONOL, DISODIUM EDTA, ETHYLPARABEN, FRAGRANCE (PARFUM), GLYCERIN, HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER, IODOPROPYNYL BUTYLCARBAMATE, ISOHEXADECANE, METHYLPARABEN, PANTHENOL, PENTYLENE GLYCOL, NIACINAMIDE, PEG-4, PEG-4 DILAURATE, PEG-4 LAURATE, PEG-100 STEARATE, POLYETHYLENE, POLYSORBATE 60, PROPYLPARABEN, STEARIC ACID, STEARYL ALCOHOL, TOCOPHERYL ACETATE, WATER (AQUA).

QUESTIONS OR COMMENTS?

1-877-932-7948

LABEL COPY

EQUALINE

EQUALINE

OCTISALATE, AVOBENZONE, HOMOSALATE, OCTOCRYLENE LOTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:41163-356
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTISALATE OCTISALATE 50 mg
AVOBENZONE AVOBENZONE 30 mg
HOMOSALATE Homosalate 30 mg
OCTOCRYLENE Octocrylene 26 mg

Inactive Ingredients

Ingredient Name Strength
ASCORBIC ACID
docosanol
BENZYL ALCOHOL
CETOSTEARYL ALCOHOL
CETEARYL GLUCOSIDE
CETYL ALCOHOL
DIMETHICONE
DIMETHICONOL (2000 CST)
EDETATE DISODIUM
ETHYLPARABEN
GLYCERIN
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%)
IODOPROPYNYL BUTYLCARBAMATE
Isohexadecane
METHYLPARABEN
PANTHENOL
PENTYLENE GLYCOL
NIACINAMIDE
POLYETHYLENE GLYCOL 200
PEG-4 DILAURATE
PEG-4 LAURATE
PEG-100 STEARATE
HIGH DENSITY POLYETHYLENE
POLYSORBATE 60
PROPYLPARABEN
STEARIC ACID
stearyl alcohol
.ALPHA.-TOCOPHEROL ACETATE
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:41163-356-06 178 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2013-03-15


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