LAXATIVES RUBILAX- psyllium huskpowder granule

LAXATIVES RUBILAX by

Drug Labeling and Warnings

LAXATIVES RUBILAX by is a Otc medication manufactured, distributed, or labeled by Lydia Co., Ltd., I World Pharmaceutical Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

psyllium husk powder, sennae fructus powder

INACTIVE INGREDIENT

lactose monohydrate, acacia, corn starch, carboxymethylcellulose calcium, l-menthol

PURPOSE

constipation

relieving the following symptoms of constipation: loss of appetite, abdominal distension, intestinal fermentation, hemorrhoids

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

adults take intake does of 3.5g twice a day morning and evening on an empty stomach, however, taking the minimum amount of the first time and watching the shape and condition of the stomach gradually increases or decreases

WARNINGS

do not administer to the following patients,

the product contains lactose, patients with rare hereditary problems of galactose intolerance, the lapp deficiency or glucose-galactose malabsorption should not take this medicine

DOSAGE & ADMINISTRATION

for oral use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

LAXATIVES RUBILAX 
psyllium huskpowder granule

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72988-0010
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PSYLLIUM HUSK (UNII: 0SHO53407G) (PSYLLIUM HUSK - UNII:0SHO53407G)	PSYLLIUM HUSK	2168 mg  in 3.5 g
SENNA PODS (UNII: S8SJ19N2NX) (SENNA PODS - UNII:S8SJ19N2NX)	SENNA PODS	496 mg  in 3.5 g

Inactive Ingredients
Ingredient Name	Strength
LEVOMENTHOL (UNII: BZ1R15MTK7)
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72988-0010-2	30 in 1 POUCH	04/22/2019
1	NDC: 72988-0010-1	3.5 g in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		04/22/2019

Labeler - Lydia Co., Ltd. (695735569)

Registrant - Lydia Co., Ltd. (695735569)

Establishment
Name	Address	ID/FEI	Business Operations
I World Pharmaceutical Co., Ltd.		688222857	manufacture(72988-0010)

Establishment
Name	Address	ID/FEI	Business Operations
Lydia Co., Ltd.		695735569	label(72988-0010)