POLYSACCHARIDE-IRON- polysaccharide-iron capsule 
Advance Pharmaceutical Inc.

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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Polysaccharide-Iron Complex 150 mg

Drug Facts

.

Active Ingredient

(in each capsule)

Iron (as Polysaccharide Iron) 150 mg

Purpose

Iron Supplement

Uses

WARNINGS

Do not exceed recommended dosage. The treatment of any anemic condition should be under the advice and supervision of a doctor. Occasional gastrointestinal discomfort (such as nausea) may be minimized by taking with meals. Iron-containing medication may occasionally cause black stools, constipation or diarrhea. If pregnant or breast feeding, ask a health professional before use.

Accidental overdose of Iron containing products is a leading cause of fatal poisoning in children under 6.

DRUG INTERACTION PRECAUSION: Since oral iron products interfere with absorption of tetracycline antibiotics, these products should not be taken within two hours of each other.

Keep out of reach of children.

In case of accidental overdose, call a doctor or poison control center immediately.

Directions

Adults only: One capsule daily or as directed by a doctor. Do not exceed recommended dosage.

Other Information

Inactive Ingredients

Microcrystalline Cellulose, geltain, corscarmellose sodium, citric acid anhydrous, stearic acid, titanium dioxide, D&C Yellow #10, sodium lauryl sulfate, FD&C Yellow #6, FD&C Red#40, FD&C Blue #1and white ink

Questions or Comments

TAMPER RESISTENT: DO NOT USE IF IMPRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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NDC

POLYSACCHARIDE-IRON 
polysaccharide-iron capsule
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:17714-077
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
IRON (UNII: E1UOL152H7) (IRON - UNII:E1UOL152H7) IRON150 mg
Inactive Ingredients
Ingredient NameStrength
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
GELATIN (UNII: 2G86QN327L)  
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
Product Characteristics
ColororangeScorescore with uneven pieces
ShapeCAPSULESize19mm
FlavorImprint Code 077
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:17714-077-01100 in 1 BOTTLE; Type 0: Not a Combination Product05/26/2015
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other05/26/2015
Labeler - Advance Pharmaceutical Inc. (078301063)

Revised: 12/2019
Document Id: 9a63cc06-6032-4c5a-e053-2a95a90aa3a3
Set id: a42168eb-180e-4b67-b8fd-641b0af32ff3
Version: 2
Effective Time: 20191223
 
Advance Pharmaceutical Inc.