NDC 64272-736 African Sea-coconut Herbal Mixture

Product Information

Product Packages

NDC 64272-736-01

Package Description: 1 BOTTLE, GLASS in 1 BOX > 177 mL in 1 BOTTLE, GLASS

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Product Details

African Sea-coconut Herbal Mixture is product labeled by Luen Fook Medicine Sdn. Bhd.. The product's dosage form is and is administered via form.


What are African Sea-coconut Herbal Mixture Active Ingredients?

The following is the list of active ingredients in this product. 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.

  • ELM (UNII: 63POE2M46Y)
  • ELM (UNII: 63POE2M46Y) (Active Moiety)


Inactive Ingredient(s)

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.

  • AMMONIUM ACETATE (UNII: RRE756S6Q2)
  • BENZOIC ACID (UNII: 8SKN0B0MIM)
  • CARAMEL (UNII: T9D99G2B1R)
  • IPECAC (UNII: 62I3C8233L)
  • LICORICE (UNII: 61ZBX54883)
  • MENTHOL (UNII: L7T10EIP3A)
  • DRIMIA INDICA BULB (UNII: IQ3O648R19)
  • SODIUM BENZOATE (UNII: OJ245FE5EU)
  • SUCROSE (UNII: C151H8M554)
  • TOLU BALSAM (UNII: TD2LE91MBE)
  • PRUNUS SEROTINA BARK (UNII: 5D48E975HA)


* Please review the disclaimer below.

African Sea-coconut Herbal Mixture Labeling and Warnings

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Table of Contents



Active Ingredients (In Each 5 Ml Tsp)



Elm 65 mg


Purpose



Demulcent


Use



for the temporary relief of minor discomfort and protection of irritated areas in sore mouth and sore throat.


Warnings



Warnings


Otc - Stop Use



Stop use and ask a doctor if sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea, or vomiting. If sore mouth symptoms do not improve in 7 days, see your doctor promptly.  These could be signs of a serious condition.


Otc - Pregnancy Or Breast Feeding



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


Otc - Keep Out Of Reach Of Children



Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.


Directions



  • use only as directed
  • adults and children 12 years and older
    take orally 2 to 4 teaspoons (10-20mL) every 4 hours, not to exceed 24 teaspoons in 24 hours.
    children 6 to under 12 yearstake 1 to 2 teaspoons (5-10mL) every 4 hours, not to exceed 12 teaspoons in 24 hours.
    children under 6 yearsconsult a doctor before use.

Other Information



store at 20-25C (68-77F)


Inactive Ingredients



ammonium acetate, benzoic acid, caramel, ipecac, licorice, menthol,  drimia Indica bulb, sodium benzoate, sucrose, tolu balsam, prunus serotina bark.


Questions?



Call weekdays from 9 AM-5 PM PST at 1-877-889-8968.


Outer Box Label



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Inner Glass Bottle Label



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* Please review the disclaimer below.