gendose - sodium chloride 1 gram tablets, usp (77333-844)

gendose - sodium chloride 1 gram tablets, usp (77333-844)
SPL v6
SPL
SPL Set ID ff376144-28a1-8811-e053-6394a90aa995
Route
oral
Published
Effective Date 2020-05-15
Document Type 34390-5 HUMAN OTC DRUG LABEL

Drug Facts

Composition & Product

Active Ingredients
chloride ion (1 g)

Identifiers & Packaging

Pill Appearance
Imprint: S13 Shape: round Color: white Size: 13 mm Score: 1
Marketing Status
otc monograph drug active Since 2020-05-15
Purpose

ELECTROLYTE REPLENISHER

Description

SODIUM CHLORIDE, USP 1.0 GRAM

Medication Information

Warnings
  • 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.
Active Ingredient

SODIUM CHLORIDE, USP 1.0 GRAM

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.
Purpose

ELECTROLYTE REPLENISHER

Directions
  • TO MAKE AN ISOTONIC SOLUTION OF SODIUM CHLORIDE, DISSOLVE 1 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 CONTAINS ANY INACTIVE INGREDIENTS.
Inactive Ingredients

NONE

Description

SODIUM CHLORIDE, USP 1.0 GRAM

Section 50565-1
  • KEEP OUT OF REACH OF CHILDREN. IN CASE OF OVERDOSE, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.
Section 51945-4

Structured Label Content

Warnings (WARNINGS)
  • 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.
Active Ingredient (ACTIVE INGREDIENT (IN EACH TABLET))

SODIUM CHLORIDE, USP 1.0 GRAM

Uses (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.
Purpose (PURPOSE)

ELECTROLYTE REPLENISHER

Directions (DIRECTIONS)
  • TO MAKE AN ISOTONIC SOLUTION OF SODIUM CHLORIDE, DISSOLVE 1 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 (OTHER INFORMATION)
  • EACH TABLET CONTAINS: SODIUM 394 MG
  • STORE AT ROOM TEMPERATURE 15° - 30°C (59° - 86°F)
  • PRODUCT DOES NOT CONTAINS ANY INACTIVE INGREDIENTS.
Inactive Ingredients (INACTIVE INGREDIENTS)

NONE

Section 50565-1 (50565-1)
  • KEEP OUT OF REACH OF CHILDREN. IN CASE OF OVERDOSE, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.
Section 51945-4 (51945-4)

Advanced Ingredient Data

Raw Label Data

All Sections (JSON)

Additional Information

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Source: dailymed · Ingested: 2026-02-15T12:06:27.713519 · Updated: 2026-03-14T23:09:15.187219