ANTIPHLAMINE- l-menthol, l-camphor, methyl salicylate lotion 
Lydia Co., Ltd.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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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

acetone, chloroxylenol, water

For external use only

label

ANTIPHLAMINE 
l-menthol, l-camphor, methyl salicylate lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72988-0028
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:72988-0028-130 g in 1 JAR; Type 0: Not a Combination Product01/02/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other01/02/2022
Labeler - Lydia Co., Ltd. (695735569)
Registrant - Lydia Co., Ltd. (695735569)
Establishment
NameAddressID/FEIBusiness Operations
Lydia Co., Ltd.695735569manufacture(72988-0028)

Revised: 7/2023
Document Id: ffb6c041-03a7-c6c1-e053-6394a90a8194
Set id: d4944ee3-23a3-f0b8-e053-2995a90a6ef1
Version: 2
Effective Time: 20230705
 
Lydia Co., Ltd.