ALLEVIA- vitamin c, d3, b1, b6, b12, folate, nadh, coenzyme q-10 tablet 
Florrax Pharmaceutical Corp.

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.

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Allevia

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

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

KEEP OUT OF REACH OF CHILDREN

Storage:

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

Manufactured for:

Florrax Pharmaceutical

Terrell, TX 75161

label

ALLEVIA 
vitamin c, d3, b1, b6, b12, folate, nadh, coenzyme q-10 tablet
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:84460-921
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ASCORBIC ACID (UNII: PQ6CK8PD0R) (ASCORBIC ACID - UNII:PQ6CK8PD0R) ASCORBIC ACID125 mg
CHOLECALCIFEROL (UNII: 1C6V77QF41) (CHOLECALCIFEROL - UNII:1C6V77QF41) CHOLECALCIFEROL12.5 ug
THIAMINE HYDROCHLORIDE (UNII: M572600E5P) (THIAMINE ION - UNII:4ABT0J945J) THIAMINE HYDROCHLORIDE25 mg
PYRIDOXAL PHOSPHATE ANHYDROUS (UNII: F06SGE49M6) (PYRIDOXAL 5-PHOSPHATE - UNII:F06SGE49M6) PYRIDOXAL PHOSPHATE ANHYDROUS12.5 mg
FOLIC ACID (UNII: 935E97BOY8) (FOLIC ACID - UNII:935E97BOY8) FOLIC ACID1.667 mg
METHYLCOBALAMIN (UNII: BR1SN1JS2W) (METHYLCOBALAMIN - UNII:BR1SN1JS2W) METHYLCOBALAMIN1 mg
NADH (UNII: 4J24DQ0916) (NADH - UNII:4J24DQ0916) NADH5 mg
COENZYME Q10, (2Z)- (UNII: U705VLF0VW) (COENZYME Q10, (2Z)- - UNII:U705VLF0VW) COENZYME Q10, (2Z)-50 mg
Inactive Ingredients
Ingredient NameStrength
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)  
Product Characteristics
Colorbrown (tan) Scoreno score
ShapeOVALSize19mm
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:84460-921-3030 in 1 BOTTLE; Type 0: Not a Combination Product02/10/202512/15/2025
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other02/10/202512/15/2025
Labeler - Florrax Pharmaceutical Corp. (119257612)
Registrant - Florrax Pharmaceutical Corp. (119257612)

Revised: 12/2025
Document Id: 460509fe-ef09-148d-e063-6394a90a2818
Set id: 2f235b67-e688-a377-e063-6394a90a6fee
Version: 3
Effective Time: 20251215
 
Florrax Pharmaceutical Corp.