Official product label reference

Mucus Relief — Bryant Ranch Prepack

This page contains 14 source sections for GUAIFENESIN, oral route. Label set c648e711-e944-4574-83b3-ccce8732384e, version 1.

Retrieved 2026-10-02 · openFDA dataset updated 2026-10-02 · Check the current DailyMed label

Label records can cover multiple strengths or package sizes. A label listing does not by itself establish FDA approval or current market availability. Check the source and application history for this specific product.

Uses described in the label

USE(S) helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive

Purpose

PURPOSE Expectorant

Dosage and administration — label text

DIRECTIONS do not crush, chew, or break tablet take with a full glass of water this product can be administered without regard for the timing of meals adults and children 12 years of age and over: 1 or 2 tablets every 12 hours. Do not exceed 4 tablets in 24 hours. children under 12 years of age: do not use

Warnings

WARNING .

Active ingredient

ACTIVE INGREDIENT(in each extended-release tablet) Guaifenesin 600 mg

Do not use

DO NOT USE for children under 12 years of age

Ask a doctor before use

ASK A DOCTOR BEFORE USE IF YOU HAVE persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema cough accompanied by too much phlegm (mucus)

When to stop use and seek help

STOP USE AND ASK A DOCTOR IF cough lasts more than 7 days, comes back, or occurs with fever, rash, or persistent headache. These could be signs of a serious illness.

Pregnancy or breast feeding

IF PREGNANT OR BREAST-FEEDING, ask a health professional before use.

Child safety

KEEP OUT OF REACH OF CHILDREN In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).

Storage and handling

OTHER INFORMATION tamper evident: do not use if seal on the bottle printed "SEALED for YOU PROTECTION" is broken or missing. store between 20 to 25°C (68 to 77°F)

Inactive ingredient

INACTIVE INGREDIENTS carbomer homopolymer, hypromellose, microcrystalline cellulose, povidone

Unclassified section

QUESTIONS? 1-800-616-2471 You may also report side effects to this phone number.

Supply and packaging

HOW SUPPLIED Guaifenesin 600 mg: color white, shape capsule and the imprint code is G233. NDC: 71335-2642-1: 30 EXTENDED RELEASE TABLETs in a BOTTLE NDC: 71335-2642-2: 20 EXTENDED RELEASE TABLETs in a BOTTLE NDC: 71335-2642-3: 60 EXTENDED RELEASE TABLETs in a BOTTLE NDC: 71335-2642-4: 40 EXTENDED RELEASE TABLETs in a BOTTLE NDC: 71335-2642-5: 14 EXTENDED RELEASE TABLETs in a BOTTLE NDC: 71335-2642-6: 6 EXTENDED RELEASE TABLETs in a BOTTLE Store between 20 to 25°C (68 to 77°F) Repackaged/Relabeled by: Bryant Ranch Prepack, Inc. Burbank, CA 91504

Official sources and product identifiers

DailyMed — complete source labelVerify the current version and original formatting, including tables and diagrams.
openFDA — structured source recordMachine-readable label source, linked by the exact label set ID.
Drugs@FDA application ANDA209215Application history where available; verify the specific product and indication.

Substances listed: GUAIFENESIN

RxNorm identifiers: 636522

Package NDC codes

71335-2642-1, 71335-2642-2, 71335-2642-3, 71335-2642-4, 71335-2642-5, 71335-2642-6

Further research and background

These are external searches for related information. Research, encyclopedia and news articles have not been imported into this product record.

Coverage and corrections

The text is extracted from a US structured product label. Tables are represented as text where supplied; formatting and illustrations may be lost. A missing section does not mean a risk is absent. This reference has not been independently reviewed by a clinician and is not a live safety-alert service.

Source retrieved 2026-10-02. Read the source policy.

Mucus Relief drug information