SOLMEET - calcium carbonate paste, dentifrice 
Solbin Co., Ltd

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Drug Facts

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

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

for dental care

keep out of reach of the children

use when is needed

- 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

apply proper amount on your toothbrush

package label
SOLMEET 
calcium carbonate paste, dentifrice
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:42352-7001
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:42352-7001-1 120 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

Revised: 12/2010
Document Id: c0412d16-9431-41bd-88af-25623de1e551
Set id: 6ddaa6a3-173a-4f42-911f-832858baa5d6
Version: 1
Effective Time: 20101222
 
Solbin Co., Ltd