AFTER CUTS AND SCRAPES- lidocaine hydrochloride, benzalkonium chloride solution

After Cuts and Scrapes by

Drug Labeling and Warnings

After Cuts and Scrapes by is a Otc medication manufactured, distributed, or labeled by Tender Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Lidocaine Hydrochloride 2.5%

Benzalkonium Chloride .13%

Purpose

Anesthetic

Antiseptic

Uses

First aid for the temporary relief of pain and to protect from infection in minor cuts, scrapes and burns

Warnings

For External Use Only

When using this Product:

• Do not get into eyes
• Do not use in large quantities, particularly over raw surfaces or blistered areas

Stop use and ask a doctor if:

• rash, redness or swelling occurs or pain increases
• in case of deep puncture wounds, animal bites or serious burns consult a doctor

If swallowed, get medical help or contact a poison control center right away

If in eyes flush with water for 15 minutes and call a doctor

Keep Out of Reach of Children

Directions

Shake Well. Clean affected area. Spray on the area 1 to 3 times daily

Adults and children 2 years and older apply to affected area

Children under 2 years ask a doctor

Inactive Ingredients

Aloe Vera Gel, Germaben II, Orange Blossom Fragrance, Polysorbate 20, Propylene Glycol, Purified Water and Sorbitol 70%

Package Label

Family Medic

After Cuts & Scrapes

Topical Analgesic/Antiseptic

First Aid Treatment Spray Formula

Family Medic

• Relieves pain from minor cuts, scrapes and burns
• Helps prevent infecction

For Cuts, Scrapes and Burns

After Cuts & Scrapes

Anesthetic, Antiseptic Spray

Medicated First Aid Treatment with Aloe Vera

Fast pain relief. Helps prevent infection & heal minor

• cuts
• burns
• scrapes
• irritations

1 fl. Oz

30mL

Tender Corporation Littleton, NH 03561 Made in USA

See a complete line of our products for the prevention and treatement of outdoor ailments at www.tendercorp.com

INGREDIENTS AND APPEARANCE

AFTER CUTS AND SCRAPES 
lidocaine hydrochloride, benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 44224-3300
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	26 mg  in 1 mL
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE HYDROCHLORIDE ANHYDROUS	25 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
SORBITOL (UNII: 506T60A25R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 44224-3300-0	1 in 1 BOX	07/11/2003
1		30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/11/2003

Labeler - Tender Corporation (064437304)

Registrant - Tender Corporation (064437304)

Establishment
Name	Address	ID/FEI	Business Operations
Tender Corporation		064437304	manufacture(44224-3300)