Active ingredient (in each 5 mL)

Guaifenesin 100 mg

Purpose

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

When using this product

Do not use more than directed

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 right away.

Directions

do not take more than 6 doses in any 24-hour period

age	dose
adults and children 12 years and over	2 to 4 teaspoonfuls every 4 hours
children 6 years to under 12 years	1 to 2 teaspoonfuls every 4 hours
children 2 to under 6 yars	1/2 to 1 teaspoonful every 4 hours
children under 2 years	ask a doctor

Other information

store at 20°-25°C (68°-77°F)
packaged with tamper evident seal under cap
each 5 mL contains: sodium 3 mg

Inactive ingredients

Caramel, citric acid anhydrous, dextrose, FD&C red #40, flavor, gylcerin, high fructose corn syrup, menthol, purified water, saccharin, sodium, sodium benzoate

Questions or Comments

1-877-250-3427

Manufactured For:
Method Pharmaceuticals, LLC
Southlake, TX 79092

LR-205

Rev-2024

HOW SUPPLIED

Guaifenesin Liquid USP 100 mg/5 mL

NDC 72162-2278-2: Bottle of 16 fl. oz. (473 mL)

Repackaged/Relabeled by:
Bryant Ranch Prepack, Inc.
Burbank, CA 91504

Guaifenesin Liquid 100 mg/5 mL

GUAIFENESIN
guaifenesin liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:72162-2278(NDC:58657-508)
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ)	GUAIFENESIN	100 mg in 5 mL

Ingredient Name	Strength
Inactive Ingredients
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
CARAMEL (UNII: T9D99G2B1R)
DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
FD&C RED NO. 40 (UNII: WZB9127XOA)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)

Product Characteristics
Color	red	Score
Shape		Size
Flavor	CHERRY	Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:72162-2278-2	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/22/2024

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M012	04/01/2024

Labeler - Bryant Ranch Prepack (171714327)

Registrant - Bryant Ranch Prepack (171714327)

Name	Address	ID/FEI	Business Operations
Establishment
Bryant Ranch Prepack		171714327	REPACK(72162-2278) , RELABEL(72162-2278)