TUSSIN ADULT MUCUS AND CHEST CONGESTION- guaifenesin liquid 
P & L Development, LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Active ingredients
(in each 10 mL)

Guaifenesin 200 mg

Purposes

Expectorant

Uses

helps loosen phlegm (mucus) and thin bronchial secretions to make coughs more productive.

Warnings

Ask a doctor before use if you have

  • cough that occurs with too much phlegm (mucus)
  • cough that lasts or is chronic such as occurs with smoking, asthma, chronic bronchitis or emphysema

Stop use and ask a doctor if

cough lasts more than 7 days, comes back, 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 (1-800-222-1222) right away.

Directions

Other information

Inactive ingredients

anhydrous citric acid, caramel, FD&C red #40, flavor, glucose, glycerin, high fructose corn syrup, menthol, purified water, saccharin sodium, sodium benzoate

Questions or comments?

 Call 1-877-753-3935 Monday-Friday 9AM-5PM EST

Principal Display Panel

Compare to the active ingredients in Robitussin® Mucus+Chest Congestion Original*

adult

tussin

mucus + chest congestion

guaifenesin 200mg

expectorant

relievies:

for ages 12 & over

non-drowsy

alcohol free

FL OZ (mL)

*This product is not manufactured or distributed by Pfizer Consumer Healthcare, distributors of Robitussin®Mucus+ Chest Congestion original.

TAMPER EVIDENT: DO NOT USE IF PRINTED  SAFETY SEAL AROUND BOTTLE OR UNDER THE CAP IS BROKEN OR MISSING.

Manufactured by:

PL Developments

11865 S. Alameda St

Lynwood, CA 90262

Package Label

Guaifenesin 200 mg

ReadyinCase Adult Tussin Mucus & Chest Congestion

TUSSIN  ADULT MUCUS AND CHEST CONGESTION
guaifenesin liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49580-0389
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN200 mg  in 10 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
GLYCERIN (UNII: PDC6A3C0OX)  
WATER (UNII: 059QF0KO0R)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
DEXTROSE (UNII: IY9XDZ35W2)  
HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)  
CARAMEL (UNII: T9D99G2B1R)  
MENTHOL (UNII: L7T10EIP3A)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49580-0389-41 in 1 BOX02/28/201512/31/2025
1118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
2NDC:49580-0389-5118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/28/201512/31/2025
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34102/28/201512/31/2025
Labeler - P & L Development, LLC (101896231)

Revised: 6/2023
Document Id: ac1e90c0-e034-4efc-a266-ef83d955d8c7
Set id: c047f474-3a91-43be-8a20-05af77c1aef8
Version: 5
Effective Time: 20230607
 
P & L Development, LLC