UP AND UP PAIN RELIEVING CLEANSING- benzalkonium chloride, lidocaine spray

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Drug Labeling and Warnings

up and up by is a Otc medication manufactured, distributed, or labeled by Target Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient

Benzalkonium Cl 0.13%w/w

Lidocaine HCl  2.5% w/w

PURPOSE

Purpose

Benzalkonium Cl 0.13% w/w ........ First aid antiseptic

Lidocaine HCl 2.5% w/w................Pain relieving spray

INDICATIONS & USAGE

Uses  first aid to help bacterial contamination or skin

infectionand for temporary relief of of pain and itching associated

with minor  cuts  scrapes  burns  sunburn  skin irritations

WARNINGS

Warnings

For external use only.

Do not use if you have ever had an allergic reaction to this

product or any of its ingredients.

Ask a doctor before use if you have deep or puncture wounds

animal bites  serious burns.

When using this product do not use in or near eyes do not

apply over large areas of the body or in large quantities do not apply

over raw surfaces or blistered areas.

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.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a

Poison Control Center right away.

DOSAGE & ADMINISTRATION

Directions  adults and children 2 years and older  clean the affected

area; spray a small amount on the area 1-3 times daily may be covered

with a sterile bandage (let dry first) children under 2 years, ask a doctor

STORAGE AND HANDLING

Other information  avoid excessive heat

INACTIVE INGREDIENT

Inactive ingredients  disodium

EDTA, fragrance, nonoxyl-9, propylene

glycol, water.

QUESTIONS

Questions?  Call 1-800-910-6874

DESCRIPTION

helps relieve pain on contact

antiseptic helps prevent infection

no sting

antiseptic anesthetic

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

UP AND UP  PAIN RELIEVING CLEANSING
benzalkonium chloride, lidocaine spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11673-564
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	.192 g  in 147.8 mL
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	3.695 g  in 147.8 mL

Inactive Ingredients
Ingredient Name	Strength
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
NONOXYNOL-9 (UNII: 48Q180SH9T)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11673-564-01	147.8 mL in 1 PACKAGE; Type 0: Not a Combination Product	11/22/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	11/22/2017

Labeler - Target Corporation (006961700)