RIGHT REMEDIES NIGHTTIME SEVERE COLD AND FLU SOFTGEL- acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, phenylephrine hydrochloride capsule, liquid filled

RIGHT REMEDIES NIGHTTIME SEVERE COLD AND FLU softgel by

Drug Labeling and Warnings

RIGHT REMEDIES NIGHTTIME SEVERE COLD AND FLU softgel by is a Otc medication manufactured, distributed, or labeled by Strive Pharmaceuticals Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredients (in each softgel)

Acetaminophen 325 mg
Dextromethorphan HBr 10 mg
Doxylamine succinate 6.25 mg
Phenylephrine HCl 5 mg

Purposes

Pain reliever/fever reducer
Cough suppressant
Antihistamine
Nasal decongestant

Uses

 temporarily relieves common cold/flu symptoms:
    nasal congestion  sinus congestion & pressure 
    cough due to minor throat & bronchial irritation 
    cough to help you sleep  minor aches & pains 
    headache  fever  sore throat
 runny nose & sneezing  reduces swelling of nasal passages
 temporarily restores freer breathing through the nose
 promotes nasal and/or sinus drainage

Warnings

Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take  more than 8 softgels in 24 hours, which is the maximum daily amount for this product  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  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.

Ask a doctor before use if you have  liver disease  heart disease   high blood pressure  thyroid disease  diabetes  glaucoma   cough that occurs with too much phlegm (mucus)  a breathing problem or chronic cough that lasts or as occurs with smoking, asthma, chronic bronchitis, or emphysema  trouble urinating due to enlarged prostate gland

Ask a doctor or pharmacist before use if you are  taking sedatives or tranquilizers  taking the blood thinning drug warfarin

When using this product  do not use more than directed
 excitability may occur, especially in children  marked drowsiness may occur  avoid alcoholic drinks  be careful when driving a motor vehicle or operating machinery  alcohol, sedatives, and tranquilizers may increase drowsiness

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. 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  do not exceed 8 softgels 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

Other information 

store at controlled room temperature 20–25°C (68–77°F)  protect from light, heat, and moisture

Inactive ingredients

D&C Yellow No.10, FD&C Blue No.1, gelatin, glycerin, polyethylene glycol, povidone, propylene glycol, sorbitol sorbitan solution, titanium dioxide

Questions or comments?

1-888-577-8033 Monday - Friday 8am - 4pm EST

SPL UNCLASSIFIED SECTION

Compare to the active ingredients in Vicks® NyQuil™ Severe Cold & Flu LiquiCaps™*

MAX STRENGTH

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

*This product is not manufactured or distributed by The Procter & Gamble Company, owner of the registered trademarks Vicks® NyQuil™ LiquiCaps™.

Distributed by: Strive Pharmaceuticals Inc., East Brunswick, NJ 08816

PRODUCT OF INDIA

Packaging

INGREDIENTS AND APPEARANCE

RIGHT REMEDIES NIGHTTIME SEVERE COLD AND FLU SOFTGEL 
acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, phenylephrine hydrochloride capsule, liquid filled

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70692-837
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D)	ACETAMINOPHEN	325 mg
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS)	DEXTROMETHORPHAN HYDROBROMIDE	10 mg
DOXYLAMINE SUCCINATE (UNII: V9BI9B5YI2) (DOXYLAMINE - UNII:95QB77JKPL)	DOXYLAMINE SUCCINATE	6.25 mg
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV)	PHENYLEPHRINE HYDROCHLORIDE	5 mg

Inactive Ingredients
Ingredient Name	Strength
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
GELATIN, UNSPECIFIED (UNII: 2G86QN327L)
GLYCERIN (UNII: PDC6A3C0OX)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SORBITOL (UNII: 506T60A25R)
SORBITAN (UNII: 6O92ICV9RU)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Product Characteristics
Color	green	Score	no score
Shape	OVAL	Size	18mm
Flavor		Imprint Code	A07
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70692-837-84	48 in 1 BOTTLE; Type 0: Not a Combination Product	09/23/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M012	09/23/2025

Labeler - Strive Pharmaceuticals Inc. (080028013)