Geri-Tussin

Manufacturer
REMEDYREPACK INC.
Effective date
2021-03-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:49:17

Label at a glance#

ProductGeri-Tussin
Active ingredientGUAIFENESIN
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

In each 5 mL teaspoonful

Guaifenesin - 100 mg

OTC - PURPOSE SECTION

Purpose

Expectorant

INDICATIONS & USAGE SECTION

Uses

  • helps loosen phlegm (mucus) and thin bronchial secretions to make coughs more productive

WARNINGS SECTION

Warnings

Do not use

  • if you ever had an allergic reaction to any of the ingredients in this product

Ask a doctor before use if you have

  • cough that occurs with too much phlegm (mucus)
  • cough that lasts or is chronic such as occurs with smoking, asthma, chronic bronchitis, or emphysema

Stop use and ask a doctor if cough lasts more than 7 days, comes back or is accompanied by fever, rash, or persistent headache. These could be signs of a serious condition.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away

DOSAGE & ADMINISTRATION SECTION

Directions

  • do not take more than 6 doses in a 24 hour period
  • do not exceed recommended dose
 adults and children 12 years and over 2 to 4 teaspoonfuls every 4 hours
 children under 12 years ask a doctor

INACTIVE INGREDIENT SECTION

Inactive ingredients: artificial and natural cherry flavor, citric acid, FD&C red #40, menthol, methylparaben, propylene glycol, propylparaben, purified water, sodium citrate, sucralose

OTC - QUESTIONS SECTION

Questions or comments? 1-800-540-3765

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DRUG: Geri-Tussin

GENERIC: Guaifenesin

DOSAGE: LIQUID

ADMINSTRATION: ORAL

NDC: 70518-3045-0

NDC: 70518-3045-1

PACKAGING: 20 mL in 1 CUP, UNIT-DOSE

OUTER PACKAGING: 10 in 1 BOX

ACTIVE INGREDIENT(S):

  • GUAIFENESIN 100mg in 5mL

INACTIVE INGREDIENT(S):

  • ANHYDROUS CITRIC ACID
  • FD&C RED NO. 40
  • MENTHOL
  • METHYLPARABEN
  • PROPYLENE GLYCOL
  • PROPYLPARABEN
  • WATER
  • SODIUM CITRATE
  • SUCRALOSE

Remedy_LabelRemedy_Label

MM2MM2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70518-3045-02023-10-16C16284748780-1f386c649-f571-0266-e053-dadaa90a7c1ae1826732-1ae8-43d0-b2a8-48b2ce2fd336
70518-3045-02023-01-30C16284748780-1f386c649-f571-0266-e053-dadaa90a7c1ae1826732-1ae8-43d0-b2a8-48b2ce2fd336

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
57896-693-04ML - Milliliter57896-6937f25273f-d1fc-439d-af72-925bd830bb4a12024-07-12
57896-693-08ML - Milliliter57896-693b5c35bb9-0318-4e23-b8fd-dff274ac9d7012026-01-08
57896-693-16ML - Milliliter57896-6936f03e183-fd4e-458d-b2ab-ebe17daac28b12019-09-05

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70518-304570518-3045-1, 70518-3045-0
57896-693

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Geri-TussinGUAIFENESINGeri-Care Pharmaceuticals, Corp65545ca3-4e93-4b59-9e17-4742e086e8e72025-12-31WarningsExact identifier
ndc (product): 57896-693
f1d575d3-3336-b9b1-e053-2a95a90acf71e1826732-1ae8-43d0-b2a8-48b2ce2fd3362023-01-09WarningsExact identifier
spl set id: e1826732-1ae8-43d0-b2a8-48b2ce2fd336

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.