ASCORBIC ACID by Deseret Biologicals, Inc. / Apotheca Company ASCORBIC ACID liquid

ASCORBIC ACID by

Drug Labeling and Warnings

ASCORBIC ACID by is a Homeopathic medication manufactured, distributed, or labeled by Deseret Biologicals, Inc., Apotheca Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT:

ASCORBIC ACID 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C

INDICATIONS:

For temporary relief of symptoms of Vitamin C deficiency such as lack of energy, weakness, swollen and tender joints.

WARNINGS:

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

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

Tamper seal: "Sealed for Your Protection."

Do not use if seal is broken or missing.

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:

1-10 drops under the tongue, 2 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

INDICATIONS:

For temporary relief of symptoms of Vitamin C deficiency such as lack of energy, weakness, swollen and tender joints.

INACTIVE INGREDIENTS:

Demineralized Water, 25% Ethanol

QUESTIONS:

Dist. By: Deseret Biologicals, Inc.

469 W. Parkland Drive

Sandy, UT 84070 www.desbio.com

PACKAGE LABEL DISPLAY:

DESBIO

NDC: 43742-0561-1

HOMEOPATHIC

ASCORBIC ACID

1 FL OZ (30 ml)

INGREDIENTS AND APPEARANCE

ASCORBIC ACID 
ascorbic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 43742-0561
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASCORBIC ACID (UNII: PQ6CK8PD0R) (ASCORBIC ACID - UNII:PQ6CK8PD0R)	ASCORBIC ACID	6 [hp_X]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 43742-0561-1	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	01/19/2015	07/27/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		01/19/2015	07/27/2022

Labeler - Deseret Biologicals, Inc. (940741853)

Registrant - Apotheca Company (844330915)

Establishment
Name	Address	ID/FEI	Business Operations
Apotheca Company		844330915	manufacture(43742-0561) , api manufacture(43742-0561) , label(43742-0561) , pack(43742-0561)