After Burn by Adventure Ready Brands After Burn

After Burn by

Drug Labeling and Warnings

After Burn by is a Otc medication manufactured, distributed, or labeled by Adventure Ready Brands. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

AFTER BURN- lidocaine hydrochloride gel 
Adventure Ready Brands

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After Burn

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 use in large quantities, particularly over raw surfaces or blistered areas
• do not use longer than 1 week unless directed by a doctor

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.

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 
lidocaine hydrochloride gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 90107-5120
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
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)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 90107-5120-1	1 in 1 BOX	09/01/2020
1		59 mL in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 90107-5120-0	118 mL in 1 TUBE; Type 0: Not a Combination Product	09/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	09/01/2020	12/27/2024

Labeler - Adventure Ready Brands (064437304)

Registrant - Adventure Ready Brands (064437304)

Establishment
Name	Address	ID/FEI	Business Operations
Adventure Ready Brands		064437304	manufacture(90107-5120)

Revised: 12/2024

Document Id: 2a462e60-6356-f791-e063-6294a90a62e3

34390-5

Set id: afd4fbe8-2b5d-300e-e053-2995a90a0c65

Version: 2

Effective Time: 20241227