POLYSACCHARIDE-IRON capsule

Polysaccharide-Iron by

Drug Labeling and Warnings

Polysaccharide-Iron by is a Otc medication manufactured, distributed, or labeled by Advance Pharmaceutical Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

.

Active Ingredient

(in each capsule)

Iron (as Polysaccharide Iron) 150 mg

Purpose

Iron Supplement

Uses

• Iron Supplement

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

• store at 15-30 °C (59-86 °F). Do not expose to excessive heat or moisture.

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

NDC

INGREDIENTS AND APPEARANCE

POLYSACCHARIDE-IRON 
polysaccharide-iron capsule

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 17714-077
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
IRON (UNII: E1UOL152H7) (IRON - UNII:E1UOL152H7)	IRON	150 mg

Inactive Ingredients
Ingredient Name	Strength
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
Color	orange	Score	score with uneven pieces
Shape	CAPSULE	Size	19mm
Flavor		Imprint Code	077
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 17714-077-01	100 in 1 BOTTLE; Type 0: Not a Combination Product	05/26/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		05/26/2015

Labeler - Advance Pharmaceutical Inc. (078301063)