Equate Adult Tussin DM Max Daytime Nighttime

Manufacturer
Wal-Mart Stores Inc
Effective date
2020-12-23
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 23:00:23

Label at a glance#

ProductEquate Adult Tussin DM Max Daytime Nighttime
Active ingredientDEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, DOXYLAMINE SUCCINATE
Label structure23 sections

Indications and uses

• temporarily relieves cough due to minor throat and bronchial irritation as may occur with a cold • helps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes

Dosage and administration

• shake well before using • do not take more than 6 doses in any 24-hour period • measure only with dosing cup provided • keep dosing cup with product • mL = milliliter • this adult product is not intended for use in children under 12 years of age age dose adults and children 12 years and over 10 mL every 4 hours children under 12 years do not use

Storage and handling

• each 10 mL contains: sodium 7 mg • store at 20-25 ° C (68-77 ° F). Do not refrigerate.

Label contents#

Full prescribing information#

Active ingredients (in each 10 mL) - Daytime

OTC - ACTIVE INGREDIENT SECTION

Dextromethorphan HBr, USP 20 mg

Guaifenesin, USP 400 mg

Active ingredients (in each 10 mL) - Nighttime

OTC - ACTIVE INGREDIENT SECTION

Dextromethorphan HBr, USP 30 mg

Doxylamine succinate, USP 12.5 mg

Purposes - Daytime

OTC - PURPOSE SECTION

Cough suppressant

Expectorant

Purposes - Nighttime

OTC - PURPOSE SECTION

Cough suppressant

Antihistamine

Uses - Daytime

INDICATIONS & USAGE SECTION

  • temporarily relieves cough due to minor throat and bronchial irritation as may occur with a cold
  • helps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes

Uses - Nighttime

INDICATIONS & USAGE SECTION

  • temporarily relieves cough due to minor throat and bronchial irritation as may occur with a cold
  • temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
  • runny nose
  • sneezing
  • itchy, watery eyes
  • itching of the nose or throat
  • controls the impulse to cough to help you sleep

Do not use - Daytime

OTC - DO NOT USE SECTION

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.

Do not use - Nighttime

OTC - DO NOT USE SECTION

  • to make a child sleepy
  • 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 - Daytime

OTC - ASK DOCTOR SECTION

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

Ask a doctor before use if you have - Nighttime

OTC - ASK DOCTOR SECTION

  • trouble urinating due to an enlarged prostate gland
  • glaucoma
  • cough that occurs with too much phlegm (mucus)
  • a breathing problem such as emphysema or chronic bronchitis
  • persistent or chronic cough such as occurs with smoking, asthma, or emphysema

Ask a doctor or pharmacist before use if you are - Nighttime

OTC - ASK DOCTOR/PHARMACIST SECTION

taking sedatives or tranquilizers

When using this product - Nighttime

OTC - WHEN USING SECTION

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

Stop use and ask a doctor if

OTC - STOP USE SECTION

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

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions - Daytime

DOSAGE & ADMINISTRATION SECTION

  • shake well before using
  • do not take more than 6 doses in any 24-hour period
  • measure only with dosing cup provided
  • keep dosing cup with product
  • mL = milliliter
  • this adult product is not intended for use in children under 12 years of age

age

dose

adults and children

12 years and over

10 mL

every 4 hours

children under 12 years

do not use

Directions - Nighttime

DOSAGE & ADMINISTRATION SECTION

  • measure only with dosing cup provided
  • keep dosing cup with product
  • mL = milliliter
  • do not take more than 4 doses in any 24-hour period
  • this adult product is not intended for use in children under 12 years of age

age

dose

adults and children

12 years and over

10 mL

every 6 hours

children under 12 years

do not use

Other information - Daytime

STORAGE AND HANDLING SECTION

  • each 10 mL contains: sodium 7 mg
  • store at 20-25°C (68-77°F). Do not refrigerate.

Other information - Nighttime

STORAGE AND HANDLING SECTION

  • each 10 mL contains: sodium 8 mg
  • store at 20-25°C (68-77°F)

Inactive ingredients - Daytime

INACTIVE INGREDIENT SECTION

anhydrous citric acid, D&C red no. 33, FD&C red no. 40, flavor, glycerin, high fructose corn syrup, menthol, microcrystalline cellulose and carboxymethylcellulose sodium, polyethylene glycol, povidone, propylene glycol, purified water, saccharin sodium, sodium benzoate, sorbitol solution, xanthan gum

Inactive ingredients - Nighttime

INACTIVE INGREDIENT SECTION

anhydrous citric acid, FD&C red #40, flavor, glycerin, high fructose corn syrup, menthol, propylene glycol, purified water, sodium benzoate, sodium citrate, sucralose, xanthan gum

Questions or comments?

OTC - QUESTIONS SECTION

1-888-287-1915

Package/Label Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DAY & NIGHT RELIEF VALUE PACK

Compare to Robitussin® Maximum Strength Cough + Chest Congestion DM Active Ingredients

Non-Drowsy/Maximum Strength

Adult

Tussin DM

Max

Daytime

Cough & Chest Congestion DM

Dextromethorphan HBr – Cough Supressant

Guaifenesin – Expectorant

Peak Cold

Relief of:

Cough

Mucus

Chest congestion

Ages 12+

Alcohol-Free

Gluten-Free

DM MAX

Dosage Cup Included

TOTAL 8 FL OZ (236 mL) – 2 x 4 FL OZ (118 mL)

DAY & NIGHT RELIEF VALUE PACK

Compare to Robitussin® Maximum Strength Nighttime Cough DM Active Ingredients

Maximum Strength

Adult

Tussin DM

Max

Nighttime

Nighttime Cough DM

Dextromethorphan HBr – Cough Suppressant

Doxylamine Succinate – Antihistamine

Relief of:

Cough

Itchy throat

Runny Nose

Ages 12+

Alcohol-Free

Gluten-Free

DM MAX

Dosage Cup Included

TOTAL 8 FL OZ (236 mL) – 2 x 4 FL OZ (118 mL)

Adult Tussin DM Max Carton Image 1
Adult Tussin DM Max Carton Image 1
Adult Tussin DM Max Carton Image 2
Adult Tussin DM Max Carton Image 2

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
49035-799-26ML - Milliliter49035-79986325995-3070-420c-830d-91ce2cbc19a912013-07-02

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 28 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49035-60649035-606-12
49035-79949035-799-26

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 31 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
3fef78ad-8716-4ce9-a19f-fd7fb2f8101db6725cc2-d26c-472f-a0ec-c316db82747b2020-12-23WarningsExact identifier
spl id: 3fef78ad-8716-4ce9-a19f-fd7fb2f8101d
spl set id: b6725cc2-d26c-472f-a0ec-c316db82747b

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.