Health Mart 44-730-Delisted

Daytime by

Drug Labeling and Warnings

Daytime by is a Otc medication manufactured, distributed, or labeled by Strategic Sourcing Services, LLC (Health Mart), LNK International, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DAYTIME- acetaminophen, dextromethorphan hbr, phenylephrine hcl capsule, liquid filled 
Strategic Sourcing Services, LLC (Health Mart)

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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Health Mart 44-730-Delisted

Active ingredients (in each liquid-filled capsule)

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 and flu symptoms:
    • sore throat
    • nasal congestion
    • headache
    • fever
    • minor aches and pains
    • cough due to minor throat and bronchial irritation 

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, persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea, or vomiting, consult a doctor promptly.

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

Ask a doctor before use if you have

  • liver disease
  • thyroid disease
  • diabetes
  • persistent or chronic cough such as occurs with smoking, asthma, or emphysema
  • heart disease
  • high blood pressure
  • cough that occurs with too much phlegm (mucus)
  • difficulty in urination due to enlargement of the prostate gland

Ask a doctor or pharmacist before use if you are

taking the blood thinning drug warfarin. 

When using this product

do not exceed recommended dosage. 

Stop use and ask a doctor if

  • nervousness, dizziness, or sleeplessness occur
  • 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.

In case of accidental overdose, get medical help or contact a Poison Control Center right away. Prompt medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

Directions

  • do not take more than directed
  • do not take more than 8 capsules per 24 hours
  • adults and children 12 years and over: take 2 capsules with water every 4 hours
  • children under 12 years: ask a doctor

Other information

  • TAMPER EVIDENT: DO NOT USE IF OUTER PACKAGE IS OPENED OR BLISTER IS TORN OR BROKEN
  • store at 25°C (77°F); excursions permitted between 15°-30°C (59°-86°F)
  • protect from light, heat and moisture
  • see end flap for expiration date and lot number

Inactive ingredients

FD&C red #40, FD&C yellow #6, gelatin, glycerin, isopropyl alcohol, medium chain triglycerides, polyethylene glycol, povidone, propylene glycol, purified water, sorbitol sorbitan solution, white ink

Questions or comments?

1-800-426-9391

Principal Display Panel

NDC: 62011-0457-1

HealthMart®

Compare to the active ingredients in
Vicks® DayQuil® Cold & Flu LiquiCaps®*

MULTI-SYMPTOM

Daytime Liquid Caps

Acetaminophen - Pain Reliever/Fever Reducer
Dextromethorphan HBr
- Cough Suppressant
Phenylephrine HCl
- Nasal Decongestant

Multi-Symptom Cold & Flu Relief
Headache, Fever, Sore Throat, Nasal Congestion, Cough

Non-Drowsy Antihistamine-Free

Actual Size

24 Liquid Caps

TAMPER EVIDENT: DO NOT USE IF
PACKAGE IS OPENED OR IF BLISTER
UNIT IS TORN, BROKEN OR SHOWS
ANY SIGNS OF TAMPERING

*This product is not manufactured or distributed by The Procter &
Gamble Company, owner of the registered trademark Vicks® DayQuil®
Cold & Flu LiquiCaps®.

50844               ORG012073008
Product of Dubai Packaged and Quality Assured in the USA

McKESSON
Distributed by McKesson Corporation
6555 State Highway 161
Irving, TX 75039
www.mckesson.com

PARENTS:
Learn about teen medicine abuse
www.StopMedicineAbuse.org

Healthmart 44-730

Healthmart 44-730

DAYTIME 
acetaminophen, dextromethorphan hbr, phenylephrine hcl capsule, liquid filled
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 62011-0457
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN325 mg
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE10 mg
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE5 mg
Inactive Ingredients
Ingredient NameStrength
FD&C RED NO. 40 (UNII: WZB9127XOA)  
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
GELATIN, UNSPECIFIED (UNII: 2G86QN327L)  
GLYCERIN (UNII: PDC6A3C0OX)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
SORBITOL (UNII: 506T60A25R)  
SORBITAN (UNII: 6O92ICV9RU)  
Product Characteristics
ColororangeScoreno score
ShapeOVALSize20mm
FlavorImprint Code 730
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 62011-0457-12 in 1 CARTON08/05/202008/24/2022
112 in 1 BLISTER PACK; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34108/05/202008/24/2022
Labeler - Strategic Sourcing Services, LLC (Health Mart) (116956644)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.038154464pack(62011-0457)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.832867837pack(62011-0457)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.967626305pack(62011-0457)

Revised: 8/2022
 
Strate

Trademark Results [Daytime]

Mark Image

Registration | Serial
Company
Trademark
Application Date
DAYTIME
DAYTIME
85734974 4309200 Live/Registered
Lagunitas Brewing Company
2012-09-21
DAYTIME
DAYTIME
78108756 2659705 Dead/Cancelled
Colgate-Palmolive Company
2002-02-14
DAYTIME
DAYTIME
77084896 not registered Dead/Abandoned
Paragon Vision Sciences, Inc.
2007-01-17
DAYTIME
DAYTIME
74266708 not registered Dead/Abandoned
Pfizer Inc
1992-04-17
DAYTIME
DAYTIME
74024861 not registered Dead/Abandoned
Mattel, Inc.
1990-02-02
DAYTIME
DAYTIME
73334918 1280322 Dead/Cancelled
Hearst/ABC Video Services
1981-11-02

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