SODIUM CHLORIDE 1 GRAM- sodium chloride tablet 
Gendose Pharmaceuticals, LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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GENDOSE - SODIUM CHLORIDE 1 GRAM TABLETS, USP (77333-844)

ACTIVE INGREDIENT (IN EACH TABLET)

SODIUM CHLORIDE, USP 1.0 GRAM

PURPOSE

ELECTROLYTE REPLENISHER

USES

WARNINGS

DIRECTIONS

INACTIVE INGREDIENTS

NONE

OTHER INFORMATION

01b LBL_Sodium Chloride_77333-844-10

SODIUM CHLORIDE  1 GRAM
sodium chloride tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77333-844
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE1 g
Product Characteristics
ColorwhiteScoreno score
ShapeROUNDSize13mm
FlavorImprint Code S13
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:77333-844-10100 in 1 BOX05/15/2020
1NDC:77333-844-251 in 1 BLISTER PACK; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34905/15/2020
Labeler - Gendose Pharmaceuticals, LLC (080257510)
Registrant - Gendose Pharmaceuticals, LLC (080257510)

Revised: 6/2023
Document Id: ff376144-28a2-8811-e053-6394a90aa995
Set id: ff376144-28a1-8811-e053-6394a90aa995
Version: 1
Effective Time: 20230628
 
Gendose Pharmaceuticals, LLC