Dentemp Nightmelt

Manufacturer
DOC Brands
Effective date
2026-01-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:45:56

Label at a glance#

ProductDentemp Nightmelt
Active ingredientMENTHOL
Label structure13 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Menthol 10mg

INACTIVE INGREDIENT SECTION

Xylitol, Polyvinylpyrrolidone K90, Steviol glycosides, Natural Cherry Flavoring, Carbopol 71G, Silicon Dioxide, Magnesium Stearate, Natural Red Color, Stearic Acid

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have: • persistent or chronic cough such as occurs with smoking, asthma, or emphysema • cough accompanied by excessive phlegm (mucus)

OTC - STOP USE SECTION

Stop use and ask a doctor if: • cough persists more than 1 week, tends to recur, or is accompanied by fever, rash, or persistent headache. These could be signs of a serious condition. • sore mouth does not improve in 7 days • irritation, pain, or redness persists or worsens

OTC - QUESTIONS SECTION

Questions or comments? 833-362-2763 or consumeraffairs@doc-brands.com

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breastfeeding, ask a health care professional before use. Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

WARNINGS SECTION

Sore throat warning: if sore throat is severe, persists for more than 2 days, is accompanied or followed by fever. headache, rash, swelling, nausea, or vomiting, consult a doctor promptly. These symptoms may be serious.

INSTRUCTIONS FOR USE SECTION

Directions • adults and children 5 years of age and older, apply 1 tablet and allow it to slowly dissolve. Repeat every 2 hours as needed. Place the tablet on a clean, dry finger with the colored, curved side up. Place the colored, curved side against the roof of the mouth and hold in place for 10 seconds. The tablet will begin to slowly dissolve and provide soothing relief for more than an hour. Do not remove the tablet before it dissolves. In case of discomfort, the tablet may be removed by gently peeling the tablet from the sides while washing with warm water. Do not use any instrument to remove the tablet.

OTC - PURPOSE SECTION

Purpose to aid as a cough suppressant and provide sore throat relief

INDICATIONS & USAGE SECTION

For the temporary relief of cough due to minor throat irritaion and occasional minor sore throat

DOSAGE & ADMINISTRATION SECTION

adults and children 5 years of age and older, apply 1 tablet and allow it to slowly dissolve. Repeat every 2 hours as needed up to 7 days.

Dentemp Nightmelt Cough Relief 12ct

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Dentemp Nightmelt 12ctDentemp Nightmelt 12ct

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73653-220-01Dentemp Nightmelt1 in 1 BLISTER PACKTABLET, EXTENDED RELEASE11
73653-220-12Dentemp Nightmelt12 in 1 CARTONTABLET, EXTENDED RELEASE121

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73653-22073653-220-01, 73653-220-12

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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
47d26cb5-6046-af5a-e063-6394a90a240247d26cb5-6045-af5a-e063-6394a90a24022026-01-07WarningsExact identifier
spl id: 47d26cb5-6046-af5a-e063-6394a90a2402
spl set id: 47d26cb5-6045-af5a-e063-6394a90a2402

Reported adverse events (FAERS/openFDA)#

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