Label: MUCUS- guaifenesin tablet, extended release
-
Contains inactivated NDC Code(s)
NDC Code(s): 30142-701-20 - Packager: KROGER COMPANY
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: New Drug Application
Drug Label Information
Updated February 10, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient (in each extended-release tablet)
- Purpose
- Uses
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Warnings
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)
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
- SPL UNCLASSIFIED SECTION
-
PRINCIPAL DISPLAY PANEL - 600 mg Tablet Blister Pack Carton
COMPARE TO the active ingredient of
MUCINEX®*
See back panelNDC 30142-701-20
Kroger®
OUR PHARMACIST
RECOMMENDEDMucus
Relief ERGuaifenesin 600 mg,
Extended-Release
TabletsEXPECTORANT
12
HOUR- Relieves Chest Congestion
- Thins and Loosens Mucus
- Immediate & Extended Release
actual
size20 EXTENDED-RELEASE
TABLETS -
INGREDIENTS AND APPEARANCE
MUCUS
guaifenesin tablet, extended releaseProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:30142-701 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Guaifenesin (UNII: 495W7451VQ) (Guaifenesin - UNII:495W7451VQ) Guaifenesin 600 mg Inactive Ingredients Ingredient Name Strength CARBOMER HOMOPOLYMER TYPE B (ALLYL PENTAERYTHRITOL OR ALLYL SUCROSE CROSSLINKED) (UNII: K6MOM3T5YL) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) Product Characteristics Color WHITE Score no score Shape OVAL Size 16mm Flavor Imprint Code Mxeunic;600 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:30142-701-20 1 in 1 CARTON 09/07/2017 1 20 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 NDA NDA021282 09/07/2017 Labeler - KROGER COMPANY (006999528) Establishment Name Address ID/FEI Business Operations RECKITT BENCKISER HEALTHCARE INTERNATIONAL LTD 230780363 MANUFACTURE(30142-701) , LABEL(30142-701)