MUCUS RELIEF- guaifenesin 400 mg tablet 
HealthLife of USA LLC

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Drug Facts

Active ingredient (in each tablet)

Guaifenesin 400 mg

Purpose

Expectorant

Uses

Warnings

ask a doctor before use if you have

When using this product

  • do not exceed recommended dosage
  • do not use for more than 7 days

Stop use and ask a doctor if

  • cough lasts for more than 7 days, recurs, or is accompanied by fever, rash, or persistent headache.

These could be signs of a serious condition.

If pregnant or breast-feeding,ask a health professional before use.

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center right away.

Directions:

Other information

Inactive ingredients

colloidal silicon dioxide, magnesium stearate, microcrystalline cellulose, stearic acid, sodium starch glycolate

Questions or Comments

Call toll free 1-844-832-1138 Monday through Friday 9AM – 5PM EST or www.healthlifeofusa.com

Principal Display Panel

COMPARE TO ACTIVE INGREDIENT IN Guai-Aid® 400*

Guaifenesin 400 mg

Expectorant

* This product is not manufactured or distributed by Health Products Express, Inc., owner of the registered trademark Guai-Aid® 400.

Mucus relief

MUCUS RELIEF 
guaifenesin 400 mg tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69517-119
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN400 mg
Inactive Ingredients
Ingredient NameStrength
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
Product Characteristics
ColorwhiteScoreno score
ShapeOVALSize17mm
FlavorImprint Code EB
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69517-119-2525 in 1 CARTON04/13/2016
12 in 1 POUCH; Type 0: Not a Combination Product
2NDC:69517-119-5050 in 1 CARTON04/13/2016
22 in 1 POUCH; Type 0: Not a Combination Product
3NDC:69517-119-022 in 1 POUCH04/13/2016
32 in 1 POUCH; Type 0: Not a Combination Product
4NDC:69517-119-101000 in 1 BOTTLE04/13/2016
4NDC:69517-119-05500 in 1 BOTTLE
4NDC:69517-119-1212 in 1 BOTTLE
41 in 1 CARTON; Type 0: Not a Combination Product
5NDC:69517-119-161 in 1 CARTON06/05/2017
516 in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01204/13/2016
Labeler - HealthLife of USA LLC (079656178)
Establishment
NameAddressID/FEIBusiness Operations
Elysium Pharmaceutical Ltd.915664486manufacture(69517-119)

Revised: 10/2023
Document Id: 083389ce-8dc1-a654-e063-6294a90a76fa
Set id: 20c86c98-3725-4726-b32d-9220af235f6c
Version: 5
Effective Time: 20231021
 
HealthLife of USA LLC