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NDC 62011-0377-01 Mucus Relief Extended Release 600 mg/1 Details
Mucus Relief Extended Release 600 mg/1
Mucus Relief Extended Release is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by Strategic Sourcing Services LLC. The primary component is GUAIFENESIN.
MedlinePlus Drug Summary
Guaifenesin is used to relieve chest congestion. Guaifenesin may help control symptoms but does not treat the cause of symptoms or speed recovery. Guaifenesin is in a class of medications called expectorants. It works by thinning the mucus in the air passages to make it easier to cough up the mucus and clear the airways.
Related Packages: 62011-0377-01Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Guaifenesin
Product Information
NDC | 62011-0377 |
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Product ID | 62011-0377_4d4b875c-890b-4d5d-8b32-b823557e8f0b |
Associated GPIs | 43200010007420 |
GCN Sequence Number | 071885 |
GCN Sequence Number Description | guaifenesin TAB ER 12H 600 MG ORAL |
HIC3 | B3J |
HIC3 Description | EXPECTORANTS |
GCN | 35905 |
HICL Sequence Number | 000271 |
HICL Sequence Number Description | GUAIFENESIN |
Brand/Generic | Generic |
Proprietary Name | Mucus Relief Extended Release |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | Guaifenesin |
Product Type | HUMAN OTC DRUG |
Dosage Form | TABLET |
Route | ORAL |
Active Ingredient Strength | 600 |
Active Ingredient Units | mg/1 |
Substance Name | GUAIFENESIN |
Labeler Name | Strategic Sourcing Services LLC |
Pharmaceutical Class | Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE] |
DEA Schedule | n/a |
Marketing Category | ANDA |
Application Number | ANDA207342 |
Listing Certified Through | 2024-12-31 |
Package
Package Images

NDC 62011-0377-01 (62011037701)
NDC Package Code | 62011-0377-1 |
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Billing NDC | 62011037701 |
Package | 20 BLISTER PACK in 1 CARTON (62011-0377-1) / 1 TABLET in 1 BLISTER PACK |
Marketing Start Date | 2018-09-30 |
NDC Exclude Flag | N |
Pricing Information | |
Price Per Unit | 0.32501 |
Pricing Unit | EA |
Effective Date | 2024-02-21 |
NDC Description | HM MUCUS RELIEF ER 600 MG TAB |
Pharmacy Type Indicator | C/I |
OTC | Y |
Explanation Code | 1 |
Classification for Rate Setting | G |
As of Date | 2024-02-21 |
Standard Product Labeling (SPL)/Prescribing Information SPL 45bb6fa4-91b4-4a26-8682-8228c6c7f2b8 Details
Uses
Warnings
Ask a doctor before use if you have
- persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis or emphysema
- cough accopanied by too much phlegm (mucus)
Directions
Inactive ingredients
Principal Display Panel
Compare to the active ingredient in Mucinex®*
Mucus Relief
Guaifenesin 600 mg
Expectorant
Relieves Chest Congestion
12-Hour Relief • Thins and loosens Mucus
Extended-release tablets
*This product is not manufactured or distributed by Reckitt Benckiser LLC, distributor of Mucinex®.
TAMPER EVIDENT: DO NOT USE IF BLISTER UNIT IS TORN, BROKEN OR SHOWS ANY SIGNS OF TAMPERING.
KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION.
Distributed by McKesson Corp.,
via Strategic Sourcing Services LLC,
Memphis, TN 38141
INGREDIENTS AND APPEARANCE
MUCUS RELIEF EXTENDED RELEASE
guaifenesin tablet |
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Labeler - Strategic Sourcing Services LLC (116956644) |