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#
Contacts and useful links#
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
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 73653-220-01 | Dentemp Nightmelt | 1 in 1 BLISTER PACK | TABLET, EXTENDED RELEASE | 1 | 1 | |
| 73653-220-12 | Dentemp Nightmelt | 12 in 1 CARTON | TABLET, EXTENDED RELEASE | 12 | 1 |
Products#
Every source-derived product name is available through these pages.
- Dentemp Nightmelt
- Dentemp Nightmelt Cough Relief
- XYLITOL
- STEARIC ACID
- GLUCOSYL STEVIOL
- POVIDONE K90
- MALTODEXTRIN
- CITRIC ACID
- SILICON DIOXIDE
- CHERRY
- MAGNESIUM STEARATE
- MENTHOL
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 73653-220 | 73653-220-01, 73653-220-12 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| XYLITOL | VCQ006KQ1E | IACT |
| STEARIC ACID | 4ELV7Z65AP | IACT |
| GLUCOSYL STEVIOL | TKD5UC898Q | IACT |
| POVIDONE K90 | RDH86HJV5Z | IACT |
| MALTODEXTRIN | 7CVR7L4A2D | IACT |
| CITRIC ACID | 2968PHW8QP | IACT |
| SILICON DIOXIDE | ETJ7Z6XBU4 | IACT |
| CHERRY | BUC5I9595W | IACT |
| MAGNESIUM STEARATE | 70097M6I30 | IACT |
| MENTHOL | L7T10EIP3A | ACTIB |
| CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE | 0A5MM307FC | IACT |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 47d26cb5-6046-af5a-e063-6394a90a2402 | 47d26cb5-6045-af5a-e063-6394a90a2402 | 2026-01-07 | Warnings | 47d26cb5-6046-af5a-e063-6394a90a2402 47d26cb5-6045-af5a-e063-6394a90a2402 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
