ALLEVIA- vitamin c, d3, b1, b6, b12, folate, nadh, coenzyme q-10 tablet

Allevia by

Drug Labeling and Warnings

Allevia by is a Prescription medication manufactured, distributed, or labeled by Florrax Pharmaceutical Corp.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DOSAGE & ADMINISTRATION

Usual adult dose is 1 tablet once or twice daily or as prescribed by a licensed medical practitioner.

PRECAUTIONS

Speak to a physician prior to taking if you are pregnant or lactating. Use only as directed.

WARNINGS

KEEP OUT OF REACH OF CHILDREN

Storage:

Store at controlled room temperature 15-30°C (59-86°F). Keep in a cool dry place.

SPL UNCLASSIFIED SECTION

Manufactured for:

Florrax Pharmaceutical

Terrell, TX 75161

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ALLEVIA 
vitamin c, d3, b1, b6, b12, folate, nadh, coenzyme q-10 tablet

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 84460-921
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASCORBIC ACID (UNII: PQ6CK8PD0R) (ASCORBIC ACID - UNII:PQ6CK8PD0R)	ASCORBIC ACID	125 mg
CHOLECALCIFEROL (UNII: 1C6V77QF41) (CHOLECALCIFEROL - UNII:1C6V77QF41)	CHOLECALCIFEROL	12.5 ug
THIAMINE HYDROCHLORIDE (UNII: M572600E5P) (THIAMINE ION - UNII:4ABT0J945J)	THIAMINE HYDROCHLORIDE	25 mg
PYRIDOXAL PHOSPHATE ANHYDROUS (UNII: F06SGE49M6) (PYRIDOXAL 5-PHOSPHATE - UNII:F06SGE49M6)	PYRIDOXAL PHOSPHATE ANHYDROUS	12.5 mg
FOLIC ACID (UNII: 935E97BOY8) (FOLIC ACID - UNII:935E97BOY8)	FOLIC ACID	1.667 mg
METHYLCOBALAMIN (UNII: BR1SN1JS2W) (METHYLCOBALAMIN - UNII:BR1SN1JS2W)	METHYLCOBALAMIN	1 mg
NADH (UNII: 4J24DQ0916) (NADH - UNII:4J24DQ0916)	NADH	5 mg
COENZYME Q10, (2Z)- (UNII: U705VLF0VW) (COENZYME Q10, (2Z)- - UNII:U705VLF0VW)	COENZYME Q10, (2Z)-	50 mg

Inactive Ingredients
Ingredient Name	Strength
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
MAGNESIUM STEARATE (UNII: 70097M6I30)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)

Product Characteristics
Color	brown (tan)	Score	no score
Shape	OVAL	Size	19mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84460-921-30	30 in 1 BOTTLE; Type 0: Not a Combination Product	02/10/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		02/10/2025

Labeler - Florrax Pharmaceutical Corp. (119257612)

Registrant - Florrax Pharmaceutical Corp. (119257612)