- 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
Compare to the active ingredient of Mucinex Maximum Strength Extended Release 1200 mg Tablets
NDC 21130-206-58
Signature Care
Maximum Strength Mucus Relief Max
Guaifenesin Extended-Release
Tablets 1200 mg
Expectorant
Relieves Chest Congestion
Thins and Loosens Mucuc
12 HOUR
14 EXTENDED-RELEASE TABLETS
-
INGREDIENTS AND APPEARANCE
MUCUS RELIEF MAX
guaifenesin tablet, extended releaseProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:21130-206 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 2208 (100000 MPA.S) (UNII: VM7F0B23ZI) 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:21130-206-58 2 in 1 CARTON 05/28/2018 1 7 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 05/28/2018 Labeler - Safeway (009137209)