Good Sense Daytime: Package Insert and Label Information

GOOD SENSE DAYTIME- acetaminophen, dextromethorphan hydrobromide and phenylephrine hydrochloride capsule, liquid filled
L. Perrigo Company

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.

Active ingredients (in each softgel)

Acetaminophen 325 mg

Dextromethorphan HBr 10 mg

Phenylephrine HCl 5 mg

Purpose

Pain reliever/fever reducer

Cough suppressant

Nasal decongestant

Uses

temporarily relieves common cold/flu symptoms:

nasal congestion
cough due to minor throat and bronchial irritation
sore throat
headache
minor aches and pains
fever

Warnings

Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take

more than 4,000 mg of acetaminophen in 24 hours
with other drugs containing acetaminophen
3 or more alcoholic drinks every day while using this product

Allergy alert: Acetaminophen may cause severe skin reactions. Symptoms may include:

skin reddening
blisters
rash

If a skin reaction occurs, stop use and seek medical help right away.

Sore throat warning: If sore throat is severe, lasts for more than 2 days, is accompanied or followed by fever, headache, rash, nausea, or vomiting, consult a doctor promptly.

Do not use

with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
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.
if you have ever had an allergic reaction to this product or any of its ingredients

Ask a doctor before use if you have

liver disease
heart disease
high blood pressure
thyroid disease
diabetes
trouble urinating due to an enlarged prostate gland
cough that occurs with too much phlegm (mucus)
persistent or chronic cough as occurs with smoking, asthma, or emphysema

Ask a doctor or pharmacist before use if you are

taking the blood thinning drug warfarin

When using this product

do not use more than directed

Stop use and ask a doctor if

you get nervous, dizzy or sleepless
pain, nasal congestion or cough gets worse or lasts more than 7 days
fever gets worse or lasts more than 3 days
redness or swelling is present
new symptoms occur
cough comes back or occurs with rash or headache that lasts. 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.

Overdose warning: In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222). Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

Directions

take only as directed – see overdose warning
do not exceed 4 doses per 24 hrs

adults & children 12 yrs & over

2 softgels with water every 4 hrs

children 4 to under 12 yrs

ask a doctor

children under 4 yrs

do not use

Inactive ingredients

edible ink*, FD&C red no. 40, FD&C yellow no. 6, gelatin, glycerin, polyethylene glycol, povidone, propylene glycol, purified water, sorbitol sorbitan solution *may contain this ingredient

Questions or comments?

1-800-719-9260

Principal Display Panel

Multi-Symptom Relief

GREAT SIZE FOR TRAVEL

Pain Reliever, Fever Reducer, Cough Suppressant, Nasal Decongestant

Non-Drowsy

DayTime

Cold & Flu

Actual Size

Headache, Fever, Sore Throat, Minor Aches & Pains

Nasal Congestion

Cough

Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl

Compare to active ingredients of Vicks® DayQuil® Cold & Flu

100% SATISFACTION GUARANTEED

8 Softgels

Powerful Non-Drowsy Relief

994C2-daytime
(click image for full-size original)
GOOD SENSE DAYTIME
acetaminophen, dextromethorphan hbr, phenylephrine hcl capsule, liquid filled
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:0113-0994
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ACETAMINOPHEN (ACETAMINOPHEN) ACETAMINOPHEN 325 mg
DEXTROMETHORPHAN HYDROBROMIDE (DEXTROMETHORPHAN) DEXTROMETHORPHAN HYDROBROMIDE 10 mg
PHENYLEPHRINE HYDROCHLORIDE (PHENYLEPHRINE) PHENYLEPHRINE HYDROCHLORIDE 5 mg
Inactive Ingredients
Ingredient Name Strength
FD&C RED NO. 40
FD&C YELLOW NO. 6
GELATIN, UNSPECIFIED
GLYCERIN
POLYETHYLENE GLYCOL, UNSPECIFIED
PROPYLENE GLYCOL
WATER
POVIDONE, UNSPECIFIED
SORBITOL
SORBITAN
Product Characteristics
Color ORANGE Score no score
Shape OVAL Size 20mm
Flavor Imprint Code L994
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0113-0994-53 6 BLISTER PACK in 1 CARTON contains a BLISTER PACK
1 2 CAPSULE, LIQUID FILLED in 1 BLISTER PACK This package is contained within the CARTON (0113-0994-53)
2 NDC:0113-0994-60 10 BLISTER PACK in 1 CARTON contains a BLISTER PACK
2 2 CAPSULE, LIQUID FILLED in 1 BLISTER PACK This package is contained within the CARTON (0113-0994-60)
3 NDC:0113-0994-73 8 BLISTER PACK in 1 CARTON contains a BLISTER PACK
3 2 CAPSULE, LIQUID FILLED in 1 BLISTER PACK This package is contained within the CARTON (0113-0994-73)
4 NDC:0113-0994-62 12 BLISTER PACK in 1 CARTON contains a BLISTER PACK
4 2 CAPSULE, LIQUID FILLED in 1 BLISTER PACK This package is contained within the CARTON (0113-0994-62)
5 NDC:0113-0994-51 4 BLISTER PACK in 1 CARTON contains a BLISTER PACK
5 2 CAPSULE, LIQUID FILLED in 1 BLISTER PACK This package is contained within the CARTON (0113-0994-51)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part341 01/18/2007
Labeler — L. Perrigo Company (006013346)

Revised: 02/2021 L. Perrigo Company

DrugInserts.com provides trustworthy package insert and label information about marketed drugs as submitted by manufacturers to the US Food and Drug Administration. Package information is not reviewed or updated separately by DrugInserts.com. Every individual package label entry contains a unique identifier which can be used to secure further details directly from the US National Institutes of Health and/or the FDA.

As the leading independent provider of trustworthy medication information, we source our database directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. Our material is not intended as a substitute for direct consultation with a qualified health professional.

Terms of Use | Copyright © 2023. All Rights Reserved.