ANTIPHLAMINE by I World Pharmaceutical Co., Ltd.

ANTIPHLAMINE by

Drug Labeling and Warnings

ANTIPHLAMINE by is a Otc medication manufactured, distributed, or labeled by I World Pharmaceutical Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ANTIPHLAMINE- l-menthol, l-camphor, methyl salicylate patch 
I World Pharmaceutical Co., Ltd.

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L-Menthol, L-Camphor, Methyl Salicylate

■ temporary relief aches and pains of muscles and joints associated with:

arthritis simple backache

sprains strains bruises

Keep out of reach of children

■ Adults and children 2 years of age and older: apply to the affected area no more than 3 to 4 times daily

■ children under 2 years of age: consult a doctor

Warnings

For external use only.

Flammable

■ Keep away from fire, flame, sparks and heated surfaces. Tight cap firmly.

Stop use and ask a doctor if

■ Condition worsens or symptoms persist for more than 7days or clear up and occur again within a few days

When using this product

■ Use only as direct

■ Avoid contact with eyes

■ Do not apply to wounds or damaged skin

■ Do not bandage tightly

If pregnant or breast-feeding, ask a health professional before use

Keep out of reach of children

For external use only

acetone, chloroxylenol, water

label

ANTIPHLAMINE 
l-menthol, l-camphor, methyl salicylate patch
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 73442-0010
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CAMPHOR, (-)- (UNII: 213N3S8275) (CAMPHOR, (-)- - UNII:213N3S8275) CAMPHOR, (-)-59 mg  in 1 g
LEVOMENTHOL (UNII: BZ1R15MTK7) (LEVOMENTHOL - UNII:BZ1R15MTK7) LEVOMENTHOL8 mg  in 1 g
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE46 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
ACETONE (UNII: 1364PS73AF)  
CHLOROXYLENOL (UNII: 0F32U78V2Q)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 73442-0010-27 in 1 POUCH09/09/202006/01/2025
1NDC: 73442-0010-11.433 g in 1 PATCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01709/09/202006/01/2025
Labeler - I World Pharmaceutical Co., Ltd. (688222857)
Registrant - I World Pharmaceutical Co., Ltd. (688222857)
Establishment
NameAddressID/FEIBusiness Operations
I-WORLD PHARM CO.,LTD.688222857manufacture(73442-0010)

Revised: 6/2025