COUGH CONTROL- dextromethorphan hbr capsule, liquid filled
L&R Distributors, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Select brand 44-661-Delisted

Active ingredient (in each liquid-filled capsule)

Dextromethorphan HBr, USP 15 mg

Purpose

Cough suppressant

Use

temporarily relieves cough due to minor throat and bronchial irritation as may occur with a cold

Warnings

Do not use

if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.

Ask a doctor before use if you have

a cough that occurs with too much phlegm (mucus)
a cough that lasts or is chronic as occurs with smoking, asthma, or emphysema

Stop use and ask a doctor if

cough lasts for more than 7 days, comes back, or is accompanied by fever, rash, or persistent headache. These could be signs of a serious condition.

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

do not take more than 8 capsules in any 24-hour period
this adult product is not intended for use in children under 12 years of age
adults and children 12 years and over: take 2 capsules every 6 to 8 hours, as needed
children under 12 years: do not use

Other information

store at 25ºC (77ºF); excursions permitted between 15º-30ºC (59º-86ºF)
avoid excessive heat above 40ºC (104ºF)
protect from light
see bottle for lot number and expiration date

Inactive ingredients

edible white ink, FD&C blue #1, FD&C red #40, gelatin, glycerin, lecithin, mineral oil, polyethylene glycol, povidone, propylene glycol, purified water, sorbitol

Questions or comments?

1-800-426-9391

Principal Display Panel

Non-Drowsy
Formula

NDC 15127-661-20

select brand®
the lower price name brand

COUGH
CONTROL

Dextromethorphan HBr, USP 15 mg
Cough Suppressant

Liquidgels

*Compare to the Active Ingredient in Robitussin® CoughGels®

Easy-to-Swallow
Liquid-Filled
Capsules

8-Hour
Cough
Relief

20
Liquidgels
(Liquid-Filled
Capsules)

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

*This product is not manufactured or distributed by
Pfizer Consumer Healthcare, owner of the registered
trademark Robitussin® CoughGels®.
50844
ORG101466109
Product of China
Packaged and Quality
Assured in the USA

Distributed by:
SELECT BRAND®
DISTRIBUTORS
Pine Bluff, AR 71603
USA
AC (870) 535-3635

Select Brand 44-661

COUGH CONTROL
dextromethorphan hbr capsule, liquid filled

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:15127-661
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS)	DEXTROMETHORPHAN HYDROBROMIDE	15 mg

Ingredient Name	Strength
Inactive Ingredients
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C RED NO. 40 (UNII: WZB9127XOA)
GELATIN, UNSPECIFIED (UNII: 2G86QN327L)
GLYCERIN (UNII: PDC6A3C0OX)
MINERAL OIL (UNII: T5L8T28FGP)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
SORBITOL (UNII: 506T60A25R)
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)

Product Characteristics
Color	RED (clear red)	Score	no score
Shape	OVAL	Size	10mm
Flavor		Imprint Code	661
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:15127-661-20	1 in 1 PACKAGE	03/01/2015	09/10/2021
1		20 in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC MONOGRAPH FINAL	part341	03/01/2015	09/10/2021

Labeler - L&R Distributors, Inc. (012578514)

Name	Address	ID/FEI	Business Operations
Establishment
LNK International, Inc.		038154464	PACK(15127-661)

Name	Address	ID/FEI	Business Operations
Establishment
LNK International, Inc.		967626305	PACK(15127-661)

Name	Address	ID/FEI	Business Operations
Establishment
LNK International, Inc.		868734088	PACK(15127-661)

Revised: 7/2019

Document Id: 9e576dd3-ba02-4193-9c65-b22682f42775

Set id: 84a3966c-9ee1-43fa-92cd-c53bb5a6af01

Version: 7

Effective Time: 20190722

L&R Distributors, Inc.