FIRST SALT AFTER RAIN GRAY SALT TOOTHPASTE- calcium carbonate paste, dentifrice 
IMJACOMPANY.CO

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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ACTIVE INGREDIENT

CALCIUM CARBONATE 38.0%

Inactive ingredients

Sorbitol, Water, Glycerin, Sodium Lauryl Sulfate, PEG-32, Cellulose Gum, Sodium Saccharin, Mentha Piperita Oil, Silica, Titanium Dioxide, Sodium Benzoate, Sodium Chloride, Dicalcium Phosphate Dihydrate, Menthol, 6-Aminocaproic Acid, Alcloxa, Xylitol, Ascorbic Acid

PURPOSE

Anti-carries

WARNINGS

Keep out of the reach of children under 6 years of age.

If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

KEEP OUT OF REACH OF CHILDREN

Keep out of the reach of children under 6 years of age.

Uses

helps protect against cavities.

Directions

■ adults and children 2 years of age and older : brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or physician
■ children 2 to 6 years : use only a pea sized amount and supervise child's brushing and rinsing (to minimize swallowing)
■ children under 2 years : ask a dentist or physician

Other Information

Do not store this product in an inappropriate place such as high or low temperatures or under direct sun light.

Questions

https://firstsalt.kr
+82 80-262-3800

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of carton

FIRST SALT AFTER RAIN GRAY SALT TOOTHPASTE 
calcium carbonate paste, dentifrice
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83876-010
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CATION38.0 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
Sorbitol (UNII: 506T60A25R)  
Water (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:83876-010-021 in 1 CARTON12/01/2023
1NDC:83876-010-01120 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other12/01/2023
Labeler - IMJACOMPANY.CO (695928991)
Registrant - IMJACOMPANY.CO (695928991)
Establishment
NameAddressID/FEIBusiness Operations
DONG IL PHARMS CO., LTD.557810721manufacture(83876-010)

Revised: 1/2024
Document Id: e11296ba-6e5d-4c1f-a8b7-df3275f439cb
Set id: 2495eaca-e6cd-48e1-8f52-ab8dac233819
Version: 1
Effective Time: 20240111
 
IMJACOMPANY.CO