Label: EQUATE MUCUS RELIEF- guaifenesin tablet, extended release
- NDC Code(s): 49035-284-48, 49035-284-58
- Packager: Wal-Mart Stores, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated April 9, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT(in each extended-release tablet)
- PURPOSE
- USE(S)
- WARNING
- DO NOT USE
- ASK A DOCTOR BEFORE USE IF YOU HAVE
- STOP USE AND ASK A DOCTOR IF
- IF PREGNANT OR BREAST-FEEDING,
- KEEP OUT OF REACH OF CHILDREN
- DIRECTIONS
- OTHER INFORMATION
- INACTIVE INGREDIENTS
- QUESTIONS?
-
PRINCIPAL DISPLAY PANEL
NDC49035-284-58
equateTM
Compare to Mucinex® Extended Release 1200 mg Tablets active ingredient*
Mucus Relief Max
Guaifenesin Extended-Release Tablets 1200 mg
MAXIMUM STRENGTH
Expectorant
- Relieves Chest Congestion
- Thins and Loosens Mucus
12 HOUR
1200 mg
14 EXTENDED-RELEASE TABLETS
NDC49035-284-48
equateTM
Compare to Mucinex® Extended Release 1200 mg Tablets active ingredient*
Mucus Relief Max
Guaifenesin Extended-Release Tablets 1200 mg
MAXIMUM STRENGTH
Expectorant
- Relieves Chest Congestion
- Thins and Loosens Mucus
12 HOUR
1200 mg
28 EXTENDED-RELEASE TABLETS
-
INGREDIENTS AND APPEARANCE
EQUATE MUCUS RELIEF
guaifenesin tablet, extended releaseProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49035-284 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 1200 mg Inactive Ingredients Ingredient Name Strength CARBOMER HOMOPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: HHT01ZNK31) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) POVIDONE (UNII: FZ989GH94E) Product Characteristics Color WHITE Score no score Shape CAPSULE Size 22mm Flavor Imprint Code G234 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49035-284-58 1 in 1 CARTON 04/09/2024 1 14 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:49035-284-48 2 in 1 CARTON 04/09/2024 2 48 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 ANDA ANDA209215 04/09/2024 Labeler - Wal-Mart Stores, Inc. (051957769) Establishment Name Address ID/FEI Business Operations Guardian Drug Company 119210276 MANUFACTURE(49035-284)