Triple Complex Diabetonic: Package Insert and Label Information

TRIPLE COMPLEX DIABETONIC — potassium sulfate, sodium sulfate and tribasic calcium phosphate tablet
W LAST CC

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.

Promotes mineral balance in the blood and pancreas

Indications: Homeopathic remedy for tonic effect on the blood system and pancreas.

Dosage: Acute: Chew or dissolve 2-4 tablets in the mouth every hour for up to 10 doses or until symptoms subside. Chronic: 2-4 tablets 3 times daily.

Caution: If symptoms persist or worsen, a health care professional should be consulted.If pregnant or breastfeeding, ask a health professional before use. Keep this and all medicines from the reach of children.

Ingredients: Each dose contains equal parts of biochemic tissue salts: Kali sulph (6X) (HPUS), Nat sulphuricum (6X) (HPUS), Calc phos (6X) (HPUS)

Lactose (inactive ingredient).

If pregnant or breastfeeding, ask a health professional before use.

Contains no gluten, artificial flavors, colors or preservatives. Safe for all ages and during pregnancy.

All Native Remedies health products are especially formulated by experts in the field of natural health and are manufactured according to the highest pharmaceutical standards for maximum safety and effectiveness. For more information, visit us at www.nativeremedies.com

Distributed by

Native Remedies, LLC

6531 Park of Commerce Blvd.

Suite 160

Boca Raton, FL 33487

Phone: 1.877.289.1235

International: + 1.561.999.8857

The letters HPUS indicate that the component(s) in this product is (are) officially monographed in the Homeopathic Pharmacopoeia of the United States.

bottle label
(click image for full-size original)

TRIPLE COMPLEX DIABETONIC
kali sulph , nat sulphuricum , calc phos , lactose tablet
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:50048-043
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
POTASSIUM SULFATE (POTASSIUM CATION) POTASSIUM SULFATE 6 [hp_X]
SODIUM SULFATE (SODIUM CATION) SODIUM SULFATE 6 [hp_X]
TRIBASIC CALCIUM PHOSPHATE (CALCIUM CATION) TRIBASIC CALCIUM PHOSPHATE 6 [hp_X]
Inactive Ingredients
Ingredient Name Strength
LACTOSE
Product Characteristics
Color white (white lactose tablets) Score no score
Shape ROUND (round white lactose tablets) Size 5mm
Flavor Imprint Code
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:50048-043-60 125 TABLET (TABLET) in 1 BOTTLE, GLASS None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
UNAPPROVED DRUG PRODUCT MANUFACTURED EXCLUSIVELY FOR PRIVATE LABEL DISTRIBUTOR 01/01/2010
Labeler — W LAST CC (567284153)
Registrant — W LAST CC (567284153)
Establishment
Name Address ID/FEI Operations
W LAST CC 567284153 manufacture
Establishment
Name Address ID/FEI Operations
FEELGOOD HEALTH 538418296 relabel

Revised: 11/2011 W LAST CC

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