ABONIKI BALM - ULTRA STRENGTH TOPICAL PAIN RELIEF BALM - WHITE- camphor, eucalyptus, menthol, methyl salicylate ointment

Aboniki Balm - Ultra Strength Topical Pain Relief Balm - White by

Drug Labeling and Warnings

Aboniki Balm - Ultra Strength Topical Pain Relief Balm - White by is a Otc medication manufactured, distributed, or labeled by J C UDEOZOR & SONS GLOBAL INDUSTRIES LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Aboniki® Balm - Ultra Strength Topical Pain Relief Balm - White

Drug Facts

Drug Facts

Active Ingredients

Active Ingredients (In each gram)

Camphor 4%

Menthol 16%

Methyl Salicylate 49%

Purpose

• Active Ingredients (In each gram) ​: Purpose
• Camphor 4%: External Analgesic
• Menthol 16%: External Analgesic
• Methyl Salicylate 49%: External Analgesic

USES

Temporarily relieves minor aches & pains related to:

• arthritis
• simple backaches
• sore muscles
• joint pain
• dislocation
• leg cramps
• bruises
• sprains

Warning

For external use only.

Do not use

• on wounds or damaged skin
• with a heating pad
• if you are allergic to any of the ingredients

Ask a doctor or pharmacist before use if you have

• sensitive skin
• redness over the affected area

When using this product

• avoid contact with eyes and mucous membranes
• do not bandage tightly

Stop use and ask a doctor if

• rash, itching, or excessive irritation of the skin develops
• condition worsens or symptoms persist for more than 7 days
• symptoms 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.

Direction

• Use only as directed
• For adults and children over 12 years, apply to the affected area 3 to 4 times daily
• Wash hands after use
• For Children under 12 years, consult a doctor before use

Other Information

• Store in a cool, dry place between 20 oC to 25 oC (68 oF - 77 oF)
• Do not use if the seal is broken
• See cap for lot no, mfg, and exp date
  

Inactive Ingredients

Eucalyptus Oil, Lanolin, Microcrystalline Wax, Paraffin, Petrolatum.

Contact Info

Distributed by:

J. C. Udeozor & Sons Global Industries Limited

Email:

Info-US@aboniki.com

Mail:

300 Delaware Ave, Suite 210 #465
Wilmington, DE 19801

USA

Aboniki ® Balm - Ultra Strength Topical Pain Relief Balm - Twin Pack [Two 25g (0.88 OZ) Jar Inside]

• Aboniki ® Balm - Ultra Strength Topical Pain Relief Balm - White
• New Powerful Formula
• Fast and Deep Penetrating Pain Relief

INGREDIENTS AND APPEARANCE

ABONIKI BALM - ULTRA STRENGTH TOPICAL PAIN RELIEF BALM - WHITE 
camphor, eucalyptus, menthol, methyl salicylate ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82729-005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	160 mg  in 1 g
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)	METHYL SALICYLATE	490 mg  in 1 g
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET)	CAMPHOR (SYNTHETIC)	40 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
EUCALYPTUS OIL (UNII: 2R04ONI662)
MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
PETROLATUM (UNII: 4T6H12BN9U)
PARAFFIN (UNII: I9O0E3H2ZE)
LANOLIN (UNII: 7EV65EAW6H)

Product Characteristics
Color	white	Score
Shape		Size
Flavor	MENTHOL	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82729-005-01	25 g in 1 JAR; Type 0: Not a Combination Product	10/02/2023
2	NDC: 82729-005-02	2 in 1 CARTON	10/02/2023
2	NDC: 82729-005-01	25 g in 1 JAR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	10/02/2023

Labeler - J C UDEOZOR & SONS GLOBAL INDUSTRIES LTD (851768299)