DENTEMP CANKER COVER- canker cover tablet, extended release 
DOC Brands

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Dentemp Canker Cover 4ct

Active Ingredient (per each tablet)

Menthol 2.5 mg

Purpose

Ora pain reliever

Indications

for the temporary relief of pain associated with Canker Sores

Warnings

Do not use this product for more than 7 days unless directed by a dentist or doctor. Stop use and ask a dentist or doctor if • sore mouth symptoms do not improve in 7 days • irritation, pain or redness worsens • swelling, rash or fever develops.

Do not exceed recommended dosage.

If pregnant or breastfeeding or taking prescription drugs, ask a health care professional before use.

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

Directions

• adults and children 5 years of age and older, apply up to 3 tablets a day, as needed. Place the tablet on a clean, dry finger with the white side up. Place the white side on the sore and hold in place for 10 seconds. If sore is difficult to reach (in the fold between the cheek and gum or near the teeth or lip) break the tablet along the score and use half. Some discomfort may occur during the first few minutes, but will quickly subside, followed by hours of soothing relief. Within 30 minutes, the tablet forms a clear, gel-like bandage that seals and protects the sore for hours before dissolving. 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. • children under 5 years, ask a doctor.

Other information

store in a cool, dry place.

Inactive ingredients

annatto, carbomer homopolymer type a, citrus oil, hydroxypropyl cellulose, magnesium chloride, povidone K30, povidone K90, silicon dioxide, xylitol

Questions or comments?

833-362-2763 or consumeraffairs@doc-brands.com

Canker Cover 4ct Packaging

DENTEMP CANKER COVER 
canker cover tablet, extended release
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73653-212
Route of AdministrationORAL, TOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL2.5 mg
Inactive Ingredients
Ingredient NameStrength
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
ANNATTO (UNII: 6PQP1V1B6O)  
CARBOMER HOMOPOLYMER TYPE A (UNII: F68VH75CJC)  
CITRUS LIMON FRUIT OIL (UNII: 0HNC1J1YED)  
HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)  
POVIDONE K30 (UNII: U725QWY32X)  
POVIDONE K90 (UNII: RDH86HJV5Z)  
XYLITOL (UNII: VCQ006KQ1E)  
Product Characteristics
Colorpink (ONE SIDE PINK, ONE SIDE WHITE) Scoreno score
ShapeROUNDSize10mm
FlavorMINTImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73653-212-044 in 1 CARTON02/02/2023
1NDC:73653-212-011 in 1 BLISTER PACK; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02202/02/2023
Labeler - DOC Brands (081254601)

Revised: 12/2023
Document Id: 0cc00879-c4ab-417a-e063-6394a90a256d
Set id: f3b9c3f3-91d4-68f9-e053-2995a90a7932
Version: 2
Effective Time: 20231217
 
DOC Brands