BERKELEY AND JENSEN description, usages, side effects, indications, overdosage, supplying and lots more!

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BERKELEY AND JENSEN

BJWC
APOLLO HEALTH AND BEAUTY CARE

DRUG FACTS


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENT

BENZALKONIUM CHLORIDE 0.13%

PURPOSE

ANTIBACTERIAL

USES

HELPS ELIMINATE BACTERIA ON HANDS.

WARNINGS

FOR EXTERNAL USE ONLY.

WHEN USING THIS PRODUCT

AVOID CONTACT ITH EYES. IN CASE OF CONTACT, RINSE WITH WATER.

STOP USE AND ASK A DOCTOR IF

IRRITATION OR REDNESS DEVELOPS AND LASTS.

KEEP OUT OF REACH OF CHILDREN

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

DIRECTIONS

APPLY ONTO WET HANDS. LATHER AND RINSE THOROUGHLY.

OTHER INFORMATION

STORE AT ROOM TEMPERATURE.

INACTIVE INGREDIENTS

WATER (AQUA), COCAMIDOPROPYL BETAINE, GLYCERIN, DECYL GLUCOSIDE, HYDROXYETHYLCELLULOSE, ALOE BARBADENSIS LEAF JUICE, FRAGRANCE (PARFUM), POLOXAMER 124, POLYQUATERNIUM-7, TETRASODIUM EDTA, CITRIC ACID, SODIUM CITRATE, CAMELLIA SINENSIS LEAF EXTRACT, SACCHAROMYCES FERMENT, TOCOPHERYL ACETATE, RETINYL PALMITATE, ASCORBYL PALMITATE, NIACINAMIDE, METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE, BLUE 1 (CI 42090), RED 33 (CI 17200). 

QUESTIONS OR COMMENTS?

1-800-934-1204

LABEL IMAGE

BERKELEY AND JENSEN

BERKELEY AND JENSEN

BENZALKONIUM CHLORIDE LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:68391-149
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
benzalkonium chloride 0.13 mg

Inactive Ingredients

Ingredient Name Strength
water
COCAMIDOPROPYL BETAINE
GLYCERIN
DECYL GLUCOSIDE
HYDROXYETHYL CELLULOSE (5000 CPS AT 1%)
Aloe Vera Leaf
Poloxamer 124
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW)
EDETATE SODIUM
CITRIC ACID MONOHYDRATE
SODIUM CITRATE
GREEN TEA LEAF
SACCHAROMYCES LYSATE
.ALPHA.-TOCOPHEROL ACETATE
VITAMIN A PALMITATE
ASCORBYL PALMITATE
NIACINAMIDE
METHYLCHLOROISOTHIAZOLINONE
METHYLISOTHIAZOLINONE
FD&C BLUE NO. 1
D&C RED NO. 33

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:68391-149-50 3780 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partE part333E 2014-04-09


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