Label: ANTIPHLAMINE- l-menthol, l-camphor, methyl salicylate lotion

  • Category: HUMAN OTC DRUG LABEL

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.

Drug Label Information

Updated July 5, 2023

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

View All Sections
  • ACTIVE INGREDIENT

    L-Menthol, L-Camphor, Methyl Salicylate

  • PURPOSE

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

    • arthritis • simple backache

    • sprains • strains • bruises

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children

  • INDICATIONS & USAGE

    ■ 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

    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

  • INACTIVE INGREDIENT

    acetone, chloroxylenol, water

  • DOSAGE & ADMINISTRATION

    For external use only

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    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)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials

More Info on this Drug

Get Label RSS Feed, View NDC Code(s)NEW!