SODIUM CHLORIDE 1 GRAM- sodium chloride tablet

Drug Labeling and Warnings

Drug Details [pdf]

Drug Facts

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

Do not usewithout consulting a physician

Ask a physician before use if you havea sodium restricted diet due to multiple organ diseases

Stop use and ask a physicianif 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

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) immediately.

Directions

to make an isotonic 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

Inactive ingredients

None

Other information

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

Questions or comments?

Call 1-888-676-7161

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SODIUM CHLORIDE   1 GRAM
sodium chloride tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77333-846
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

Product Characteristics
Color	white	Score	no score
Shape	ROUND	Size	13mm
Flavor		Imprint Code	HP1
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77333-846-10	100 in 1 BOX	05/01/2026
1	NDC: 77333-846-25	10 in 1 BLISTER PACK; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M018	05/01/2026

Labeler - Gendose Pharmaceuticals, LLC (080257510)

Registrant - Gendose Pharmaceuticals, LLC (080257510)