NORMAL SALT- sodium chloride tablet

Normal Salt by

Drug Labeling and Warnings

Normal Salt by is a Otc medication manufactured, distributed, or labeled by Twin Med LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient (in each tablet)

Sodium Chloride, USP 1.0 gram

Purpose

Electrolyte Replenisher

Uses

• for the preparation of normal isotonic solution of Sodium chloride
• as an electrolyte replenisher for the prevention of heat cramps due to excessive perspiration
• any alternative use as directed by a physician

Warnings

Enter section text here

Do not use

without consulting a physician

Ask a physician before use

 if you have a sodium restricted diet due to multiple organ diseases

Stop use and ask a physician

If symptoms of heat cramps continue for more than 24 hours

If pregnant or breast-feeding

ask a health professional before use.

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center right away

Directions

• to make isontonic solution of sodium chloride, dissolve one tablet in 120 ml (four ounces) of distilled water and use as directed by a physician
• if used as an electrolyte replenisher for the prevention of heat cramps due to excessive perspiration take one tablet orally as
  directed by your physician

Other information

• each tablet contains: sodium 394 mg
• store at room temperature 15°-30°C (59°-86°F)
• product does not contain any inactive ingredients

INACTIVE INGREDIENTS

NONE

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NORMAL SALT 
sodium chloride tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55681-305
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698)	SODIUM CHLORIDE	1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Product Characteristics
Color	white	Score	no score
Shape	ROUND	Size	13mm
Flavor		Imprint Code	S13
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55681-305-03	200 in 1 BOTTLE; Type 0: Not a Combination Product	04/01/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M022	01/03/2021

Labeler - Twin Med LLC (009579330)