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integrative therapeutics
int6

US Pharmacopia NSF-GMP* Professional Brand

Science + Nature Based Nutritional Supplements

 

Vitaline® CoQ10 - 400 mg CoQ10 w/ Vitamin E - Orange Flavor

Price: $200.00 | Qty: 90 Chewable wafers | Category: CoQ10 & Ubiquinol

Vitaline was co-founded in 1972 by Jed Meese, MD, PhD who specialized in neurological, renal, and cardiovascular health. Vitaline products reflect highly specific formulas to support these systems.
Vitaline CoQ10 supports heart and brain health and is the CoQ10 used in research. This unique formulation has been proven to increase serum levels of CoQ10. In fact, Vitaline CoQ10 is searchable in WebMD and the American Family Physician.

Vitaline CoQ10 is available in:

  • 400mg (cherry vanilla, orange flavored chewable w/Vitamin E)
  • 300mg (maple flavored chewable w/Vitamin E or without)
  • 200mg (tablet, chocolate, or maple chewable w/Vitamin E)
  • 100mg (tropical, chocolate, orange or maple chewable w/Vitamin E)
  • 60mg (tablet, orange flavored chewable)

Directions and/or Dosage:

Adults chew 3 or more wafers daily or as recommended by your healthcare professional.

Ingredients:

Serving Size: 3 Chewable wafers

Ingredient Amount/Serving %DV
Calories20-
Total Carbohydrate6 g2%
Dietary Fiber<1 g4%
Sugars4 g**
Vitamin E (as dl-alpha tocopheryl acetate, d-alpha tocopherol acid succinate)600 IU2,000%
Coenzyme Q10 (CoQ10) (ubiquinone)1.2 g**

Based on 2000 calorie diet.

Other Ingredients: dextrose, fructose, cellulose, silicon dioxide, natural orange flavor, citric acid, magnesium stearate, calcium silicate, hydrogenated vegetable oil

UPC Codes: 871791003828
Product Numbers: 76239, 76239

Product Does Not Contain

  • artificial coloring
  • artificial flavoring
  • dairy products
  • gluten
  • ingredients of animal origin
  • preservatives
  • salt
  • soy
  • sucrose
  • wheat
  • yeast

Notes:

If pregnant, nursing, or taking prescription drugs, consult your healthcare professional prior to use.

*USP NSF-GMP Standards:

USP stands for the United States Pharmacopoeia. USP approval means you can be assured of purity, potency, stability and disintegration. Essentially it ensures that the product contains the ingredients listed on the label and that it has been made according to FDA Good Manufacturing Practices GMP.

  • All dietary supplement products and powders should be manufactured in a USP FDA-registered pharmaceutical facility, in compliance with Good Manufacturing Practices (GMP)
  • Ingredients all tested for purity, potency and delivery from raw materials to finished product
  • The USP specifically tests to ensure the supplement
    • Contains the ingredients listed on the label in the declared potency and amount.
    • Doesn’t contain harmful levels of specified contaminants.
    • Will break down and release into the body within a specified amount of time.
    • Has been made according to Food and Drug Administration (FDA) current Good Manufacturing Practices using sanitary and well-controlled procedures.

 

Integrative Therapeutics®, a drug-GMP audited facility, holds long-standing certifications and registrations from the following certifying organizations:

cTherapeutic Goods Administration (TGA)

bNSF - GMP Certifiation (The Public Health and Safety Company)

aGold Emerson Quality Program

 

Contact info@bravacorp.com for Drug Interactions and Recommended Dosage or contact your MD/physician.

 

FDA Required Stataement: For homeopathic products: these indications are based solely on traditional homeopathic use. They have not been evaluated by the Food & Drug Administration. For dietary supplements: This statement has not been evaluated by the Food & Drug Administration. This product is not intended to diagnose, treat, cure or prevent any disease.