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    NDC 52793-0700-10 Ahealon 30; 30; 30; 30; 30; 30; 30; 30 [kp_C]/60mL; [kp_C]/60mL; [kp_C]/60mL; [kp_C]/60mL; [kp_C]/60mL; [kp_C]/60mL; [kp_C]/60mL; [kp_C]/60mL Details

    Ahealon 30; 30; 30; 30; 30; 30; 30; 30 [kp_C]/60mL; [kp_C]/60mL; [kp_C]/60mL; [kp_C]/60mL; [kp_C]/60mL; [kp_C]/60mL; [kp_C]/60mL; [kp_C]/60mL

    Ahealon is a TOPICAL SPRAY in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by PRINCETON BIOTECHNOLOGY CORPORATION. The primary component is ALLYLTHIOUREA; ARNICA MONTANA; CALENDULA OFFICINALIS FLOWERING TOP; ECHINACEA ANGUSTIFOLIA; SILVER; ST. JOHN'S WORT; SULFUR; URTICA URENS.

    Product Information

    NDC 52793-0700
    Product ID 52793-700_6d506120-be53-45ed-a5bb-ce3c73f97003
    Associated GPIs
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    Proprietary Name Ahealon
    Proprietary Name Suffix n/a
    Non-Proprietary Name arnica montana, calendula officinalis flowering top, echinacea angustifolia, st. johns wort, silver, sulfur, allylthiourea and urtica urens
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form SPRAY
    Route TOPICAL
    Active Ingredient Strength 30; 30; 30; 30; 30; 30; 30; 30
    Active Ingredient Units [kp_C]/60mL; [kp_C]/60mL; [kp_C]/60mL; [kp_C]/60mL; [kp_C]/60mL; [kp_C]/60mL; [kp_C]/60mL; [kp_C]/60mL
    Substance Name ALLYLTHIOUREA; ARNICA MONTANA; CALENDULA OFFICINALIS FLOWERING TOP; ECHINACEA ANGUSTIFOLIA; SILVER; ST. JOHN'S WORT; SULFUR; URTICA URENS
    Labeler Name PRINCETON BIOTECHNOLOGY CORPORATION
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category UNAPPROVED HOMEOPATHIC
    Application Number n/a
    Listing Certified Through 2024-12-31

    Package

    NDC 52793-0700-10 (52793070010)

    NDC Package Code 52793-700-10
    Billing NDC 52793070010
    Package 1 BOTTLE, SPRAY in 1 CARTON (52793-700-10) / 10 mL in 1 BOTTLE, SPRAY
    Marketing Start Date 2012-04-09
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 6720fab5-6ef0-e922-0c2c-2fe5280838ab Details

    Revised: 1/2020