NDC 63479-0610 F10 Wrmlv

Agrimony,Aloe Vera,Aurum Metallicum,Azurite,Basil,Calendula Officinalis,Carica - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
63479-0610
Proprietary Name:
F10 Wrmlv
Non-Proprietary Name: [1]
Agrimony, Aloe Vera, Aurum Metallicum, Azurite, Basil, Calendula Officinalis, Carica Papaya, Cayenne, Daffodil, Dicentra Formosa, Diplacus Aurantiacus, Hibiscus Chinensis, Horse Chestnut, Hylotelephium Telephium, Lavandula Stoechas, Lilium Tigrinum, Malva Neglecta, Melilotus Alba, Nelumbo Nucifera, Phosphorus, Prunella Vulgaris, Rosa Luciae, Rosemary, Scutellaria Lateriflora, Sepia, Silicea, Thuja Occidentalis, Toxicodendron Diversilobum, Viola Odorata, Yellow Jasmine
Substance Name: [2]
Abelmoschus Moschatus Flower; Aesculus Hippocastanum Flower; Agrimonia Eupatoria Flower; Aloe Vera Flower; Azurite; Calendula Officinalis Flowering Top; Capsicum; Carica Papaya Whole; Dicentra Formosa Whole; Diplacus Aurantiacus Whole; Gelsemium Sempervirens Root; Gold; Hylotelephium Telephium Whole; Lavandula Stoechas Flowering Top; Lilium Lancifolium Whole Flowering; Malva Neglecta Whole; Melilotus Albus Top; Narcissus Pseudonarcissus Flower; Nelumbo Nucifera Flower; Ocimum Basilicum Flowering Top; Phosphorus; Prunella Vulgaris Flower; Rosa Luciae Flowering Top; Rosmarinus Officinalis Flower; Scutellaria Lateriflora Top; Sepia Officinalis Juice; Silicon Dioxide; Thuja Occidentalis Leafy Twig; Toxicodendron Diversilobum Whole; Viola Odorata Flower
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Solution/ Drops - A solution which is usually administered in a drop-wise fashion.
Administration Route(s): [4]
  • Sublingual - Administration beneath the tongue.
  • Labeler Code:
    63479
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    03-12-1996
    Listing Expiration Date: [11]
    12-31-2025
    Exclude Flag: [12]
    N
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    Product Details

    What is NDC 63479-0610?

    The NDC code 63479-0610 is assigned by the FDA to the product F10 Wrmlv which is a human over the counter drug product labeled by Apex Energetics Inc.. The generic name of F10 Wrmlv is agrimony, aloe vera, aurum metallicum, azurite, basil, calendula officinalis, carica papaya, cayenne, daffodil, dicentra formosa, diplacus aurantiacus, hibiscus chinensis, horse chestnut, hylotelephium telephium, lavandula stoechas, lilium tigrinum, malva neglecta, melilotus alba, nelumbo nucifera, phosphorus, prunella vulgaris, rosa luciae, rosemary, scutellaria lateriflora, sepia, silicea, thuja occidentalis, toxicodendron diversilobum, viola odorata, yellow jasmine. The product's dosage form is solution/ drops and is administered via sublingual form. The product is distributed in a single package with assigned NDC code 63479-0610-1 30 ml in 1 bottle, glass . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

    What are the uses for F10 Wrmlv?

    Adults & children ages 12 years and over: Take 10 drops under the tongue 3 times a day, or as directed by your healthcare professional. Consult a physician for use in children under 12 years of age.

    What are F10 Wrmlv Active Ingredients?

    An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

    Which are F10 Wrmlv UNII Codes?

    The UNII codes for the active ingredients in this product are:

    • LAVANDULA STOECHAS FLOWERING TOP (UNII: 70759G2U6A)
    • LAVANDULA STOECHAS FLOWERING TOP (UNII: 70759G2U6A) (Active Moiety)
    • LILIUM LANCIFOLIUM WHOLE FLOWERING (UNII: X67Z2963PI)
    • LILIUM LANCIFOLIUM WHOLE FLOWERING (UNII: X67Z2963PI) (Active Moiety)
    • DIPLACUS AURANTIACUS WHOLE (UNII: TO6G4140YA)
    • DIPLACUS AURANTIACUS WHOLE (UNII: TO6G4140YA) (Active Moiety)
    • MELILOTUS ALBUS TOP (UNII: 123T84GFBH)
    • MELILOTUS ALBUS TOP (UNII: 123T84GFBH) (Active Moiety)
    • ROSA LUCIAE FLOWERING TOP (UNII: 0PMA62ZZ6X)
    • ROSA LUCIAE FLOWERING TOP (UNII: 0PMA62ZZ6X) (Active Moiety)
    • PHOSPHORUS (UNII: 27YLU75U4W)
    • PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
    • AZURITE (UNII: 9AD6E582QL)
    • AZURITE (UNII: 9AD6E582QL) (Active Moiety)
    • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
    • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
    • ABELMOSCHUS MOSCHATUS FLOWER (UNII: 599O6K8K81)
    • ABELMOSCHUS MOSCHATUS FLOWER (UNII: 599O6K8K81) (Active Moiety)
    • AESCULUS HIPPOCASTANUM FLOWER (UNII: KK0Z92II8M)
    • AESCULUS HIPPOCASTANUM FLOWER (UNII: KK0Z92II8M) (Active Moiety)
    • ROSMARINUS OFFICINALIS FLOWER (UNII: NR1A27F29O)
    • ROSMARINUS OFFICINALIS FLOWER (UNII: NR1A27F29O) (Active Moiety)
    • NELUMBO NUCIFERA FLOWER (UNII: 61W322NLDV)
    • NELUMBO NUCIFERA FLOWER (UNII: 61W322NLDV) (Active Moiety)
    • SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2)
    • SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2) (Active Moiety)
    • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
    • SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
    • SCUTELLARIA LATERIFLORA TOP (UNII: C6CNB75R61)
    • SCUTELLARIA LATERIFLORA TOP (UNII: C6CNB75R61) (Active Moiety)
    • THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
    • THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)
    • HYLOTELEPHIUM TELEPHIUM WHOLE (UNII: PH797NEU5T)
    • HYLOTELEPHIUM TELEPHIUM WHOLE (UNII: PH797NEU5T) (Active Moiety)
    • TOXICODENDRON DIVERSILOBUM WHOLE (UNII: 9211E5735B)
    • TOXICODENDRON DIVERSILOBUM WHOLE (UNII: 9211E5735B) (Active Moiety)
    • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
    • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (Active Moiety)
    • CARICA PAPAYA WHOLE (UNII: S0U63B0Q51)
    • CARICA PAPAYA WHOLE (UNII: S0U63B0Q51) (Active Moiety)
    • NARCISSUS PSEUDONARCISSUS FLOWER (UNII: L879RBF1WN)
    • NARCISSUS PSEUDONARCISSUS FLOWER (UNII: L879RBF1WN) (Active Moiety)
    • DICENTRA FORMOSA WHOLE (UNII: 6OFG7K362R)
    • DICENTRA FORMOSA WHOLE (UNII: 6OFG7K362R) (Active Moiety)
    • CAPSICUM (UNII: 00UK7646FG)
    • CAPSICUM (UNII: 00UK7646FG) (Active Moiety)
    • VIOLA ODORATA FLOWER (UNII: 438W01FC7A)
    • VIOLA ODORATA FLOWER (UNII: 438W01FC7A) (Active Moiety)
    • ALOE VERA FLOWER (UNII: 575DY8C1ER)
    • ALOE VERA FLOWER (UNII: 575DY8C1ER) (Active Moiety)
    • GOLD (UNII: 79Y1949PYO)
    • GOLD (UNII: 79Y1949PYO) (Active Moiety)
    • OCIMUM BASILICUM FLOWERING TOP (UNII: 7SAB275FP2)
    • OCIMUM BASILICUM FLOWERING TOP (UNII: 7SAB275FP2) (Active Moiety)
    • AGRIMONIA EUPATORIA FLOWER (UNII: 5811MI029U)
    • AGRIMONIA EUPATORIA FLOWER (UNII: 5811MI029U) (Active Moiety)
    • MALVA NEGLECTA WHOLE (UNII: S0QQA41760)
    • MALVA NEGLECTA WHOLE (UNII: S0QQA41760) (Active Moiety)
    • PRUNELLA VULGARIS FLOWER (UNII: AT1FD041EF)
    • PRUNELLA VULGARIS FLOWER (UNII: AT1FD041EF) (Active Moiety)

    Which are F10 Wrmlv Inactive Ingredients UNII Codes?

    The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

    * Please review the disclaimer below.

    Product Footnotes

    [1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

    [2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

    [3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

    [4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

    [5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

    [8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

    [9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

    [11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

    [12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".