AFTER BURN- lidocaine hydrochloride gel

After Burn by

Drug Labeling and Warnings

After Burn 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 2.50%

Purpose

Topical Analgesic

Uses

For the temporary relief of pain due to minor burns, sunburn, minor cuts, screapes or minor skin irritations

Warnings

For external use only.

When using this product

• avoid contact with eyes
• do not used in large quantities, particularly over raw surfaces or blistered areas
• do not use longer than 1 week unless directed by a doctor
• in case of deep puncture wounds, animal bites or serious burns, consult a doctor

Stop use and ask a doctor if

• condition worsens
• symptoms persist for more than 7 days or clear up and occure again within a few days

Keep out of reach of children.

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.

Directions

Clean affected area

Adults and Children 2 years and older apply small amount to affected area not more than 3 times daily

Children under 2 years consult a doctor.

Inactive Ingredients

Aloe Vera gel, benzalkonium chloride, carbomer 980, glycerol USP, herbal fragrance, menthol, polysorbate 20, propylene glycol, purified water, and sodium hydroxide (50%)

After Burn

After Burn

Serious Treatment for Burns

Cools Burns Fast!

Advanced Pain Relief with Lidocaine HCl 2.5%

Clear Soothing Aloe Gel

Be Ready for

• Sunburns
• Scalds
• Stove Burns
• and other burns

AfterBurnRelief.com

This soothing, clear gel provides immediate pain relief from kitchen burns, sunburns or any other burns, scrapes and cuts. After Burn contains Lidocaine to relieve fain instantly and Aloe to soothe and moisturize skin.

From the makers of After Bite.

Tender Corporation Littleton NH 03561

INGREDIENTS AND APPEARANCE

AFTER BURN 
lidocaine hydrochloride gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 44224-5120
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
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)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
GLYCERIN (UNII: PDC6A3C0OX)
MENTHOL (UNII: L7T10EIP3A)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
WATER (UNII: 059QF0KO0R)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 44224-5120-0	1 in 1 BOX	11/01/2016
1		59 mL in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 44224-5120-1	1.8 mL in 1 PACKET; Type 0: Not a Combination Product	04/12/2011
3	NDC: 44224-5120-2	118 mL in 1 TUBE; Type 0: Not a Combination Product	04/12/2011

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	04/12/2011

Labeler - Tender Corporation (064437304)

Establishment
Name	Address	ID/FEI	Business Operations
Tender Corporation		064437304	manufacture(44224-5120)