SOLMEET DENTI DOCTOR- calcium carbonate paste, dentifrice

Solmeet denti doctor by

Drug Labeling and Warnings

Solmeet denti doctor by is a Otc medication manufactured, distributed, or labeled by Solbin Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient: Calcium Carbonate, Dibasic Calcium Phosphate Hydrate, Aminocarproic Acid, Aluminium Chlorohydroxy Allantoinate

INACTIVE INGREDIENT

Inactive ingredients: calcium carbonate, dibasic calcium phosphate hydrate, amonicaproic acid, aluminium chlorohydroxy allantoinate, glycerine, D-sorbitol, polyethylene glycol-1500, carboxymethylcellulose sodium, sodium lauryl sulfate, methylparaben, xylitol, L-menthol, peppermint oil, yellow no.5, blue no.1, angelica dahurica root extract, phellodendron bark extract, rosin, purified water

PURPOSE

for dental care

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

use when is needed

WARNINGS

- do not swallow when using this product
- if more than used for rinsing is accidentally swallowed, get medical helps or contact a poison control center right away

DOSAGE & ADMINISTRATION

apply proper amount on your toothbrush

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SOLMEET DENTI DOCTOR 
calcium carbonate paste, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 42352-2001
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CALCIUM CARBONATE (UNII: H0G9379FGK) (CARBONATE ION - UNII:7UJQ5OPE7D)	CALCIUM CARBONATE	15.85 g  in 100 g
DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP) (PHOSPHATE ION - UNII:NK08V8K8HR)	DIBASIC CALCIUM PHOSPHATE DIHYDRATE	0.6 g  in 100 g
AMINOCAPROIC ACID (UNII: U6F3787206) (AMINOCAPROIC ACID - UNII:U6F3787206)	AMINOCAPROIC ACID	0.05 g  in 100 g
ALCLOXA (UNII: 18B8O9DQA2) (ALCLOXA - UNII:18B8O9DQA2)	ALCLOXA	0.05 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)
SORBITOL (UNII: 506T60A25R)
POLYETHYLENE GLYCOL 1500 (UNII: 1212Z7S33A)
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
METHYLPARABEN (UNII: A2I8C7HI9T)
XYLITOL (UNII: VCQ006KQ1E)
LEVOMENTHOL (UNII: BZ1R15MTK7)
PEPPERMINT (UNII: V95R5KMY2B)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
ANGELICA DAHURICA ROOT (UNII: 1V63N2S972)
PHELLODENDRON AMURENSE BARK (UNII: PBG27B754G)
ROSIN (UNII: 88S87KL877)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 42352-2001-1	120 g in 1 TUBE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		12/15/2010

Labeler - Solbin Co., Ltd (631099371)

Registrant - Solbin Co., Ltd (631099371)

Establishment
Name	Address	ID/FEI	Business Operations
Solbin Co., Ltd		631099371	manufacture