DENTEMP NIGHTMELT- dentemp nightmelt cough relief tablet, extended release

Dentemp Nightmelt by

Drug Labeling and Warnings

Dentemp Nightmelt by is a Otc medication manufactured, distributed, or labeled by DOC Brands. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Menthol 10mg

INACTIVE INGREDIENT

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

ASK DOCTOR

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)

STOP USE

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

QUESTIONS

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

PREGNANCY OR BREAST FEEDING

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

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

WARNINGS

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

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.

PURPOSE

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

INDICATIONS & USAGE

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

DOSAGE & ADMINISTRATION

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

INGREDIENTS AND APPEARANCE

DENTEMP NIGHTMELT 
dentemp nightmelt cough relief tablet, extended release

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73653-220
Route of Administration	ORAL, TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	10 mg

Inactive Ingredients
Ingredient Name	Strength
XYLITOL (UNII: VCQ006KQ1E)
STEARIC ACID (UNII: 4ELV7Z65AP)
GLUCOSYL STEVIOL (UNII: TKD5UC898Q)
POVIDONE K90 (UNII: RDH86HJV5Z)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
CITRIC ACID (UNII: 2968PHW8QP)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
CHERRY (UNII: BUC5I9595W)
MAGNESIUM STEARATE (UNII: 70097M6I30)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)

Product Characteristics
Color	pink ((ONE SIDE PINK, ONE SIDE WHITE))	Score	score with uneven pieces
Shape	ROUND (Dome Top)	Size	13mm
Flavor	BERRY	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73653-220-12	12 in 1 CARTON	02/16/2026
1	NDC: 73653-220-01	1 in 1 BLISTER PACK; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M012	02/16/2026

Labeler - DOC Brands (081254601)