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

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KEEPAN A

Sato Pharmaceutical Co., Ltd.

DRUG FACTS




FULL PRESCRIBING INFORMATION

Active ingredient

Active ingredients
Benzalkonium chloride 0.1%
Lidocaine hydrochloride 1%

Purpose

Purpose
Benzalkonium chloride    First aid antiseptic
Lidocaine hydrochloride    External analgesic

Uses

Uses  First aid for minor cuts, scrapes and burns:
■ to help reduce the risk of infection
■ for the temporary relief of pain and itching

Warnings
For external use only

Do not use
■ in the eyes    ■ in large quantities
■ over large areas of the body    ■ over raw surfaces or blistered areas
■ longer than 1 week unless directed by a doctor

Ask a doctor before use if you have
■ deep or puncture wounds ■ animal bites ■ serious burns

When using this product
■ avoid contact with the eyes

Stop use and ask a doctor if
■ condition worsens
■ symptoms persist for more than 7 days, or clear up and occur again within a few days
■ irritation, redness, swelling or pain persists or increases or a rash or infection develops

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

Directions
Adults and children 2 years of age and older:
■ clean the affected area
■ spray a small amount directly on the affected area or apply with clean gauze or cotton saturated with KEEPAN A 1 to 3 times daily
■ may be covered with a sterile bandage
■ if bandaged, let dry first
Children under 2 years of age: Do not use, consult a doctor.

Inactive ingredients  alcohol, fragrance, hydrochloric acid, purified water, sodium chloride, sodium citrate


KEEPAN AKEEPAN A


KEEPAN A

benzalkonium chloride, lidocaine hydrochloride SPRAY

Product Information

Product Type Human otc drug label Item Code (Source) NDC:49873-019
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
benzalkonium chloride 0.1 g
LIDOCAINE HYDROCHLORIDE LIDOCAINE 1 g

Inactive Ingredients

Ingredient Name Strength
ALCOHOL
HYDROCHLORIC ACID
water
SODIUM CHLORIDE
TRISODIUM CITRATE DIHYDRATE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 60 in 1 BOTTLE, SPRAY
2 NDC:49873-019-01 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partA part333A 1981-07-15


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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