Adult Tussin Mucus and Chest Congestion DM Sugar Free by Akron Pharma Inc. / SLV PHARMACEUTICALS LLC Drug Facts

Adult Tussin Mucus and Chest Congestion DM Sugar Free by

Drug Labeling and Warnings

Adult Tussin Mucus and Chest Congestion DM Sugar Free by is a Otc medication manufactured, distributed, or labeled by Akron Pharma Inc., SLV PHARMACEUTICALS LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ADULT TUSSIN MUCUS AND CHEST CONGESTION DM SUGAR FREE- dextromethorphan hbr, guaifenesin liquid 
Akron Pharma Inc.

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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 drain bronchial tubes

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 right away (1-800-222-1222).

Directions

• do not take more than 6 doses in any 24-hour period
• mL= milliliter
• this adult product is not intended for use in children under 12 years of age
• adults and children 12 years and over: 10- 20 mL every 4 hours
• children under 12 years: do not use

Other information

• store between 20-25ºC(68-77ºF). Do not refrigerate
• protect from light
• Pharmacist-Preserve and dispense in a tight, light-resistant container with a child resistant cap as defined in the USP.

Inactive ingredients

citric acid, flavor cherry, glycerin, menthol crystals, purified water, sodium benzoate, sodium saccharin, sorbitol solution.

Questions or comments?

1-877-225-6999

ADULT TUSSIN MUCUS AND CHEST CONGESTION DM SUGAR FREE 
dextromethorphan hbr, guaifenesin liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71399-1005
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ)	GUAIFENESIN	200 mg  in 10 mL

Inactive Ingredients
Ingredient Name	Strength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
GLYCERIN (UNII: PDC6A3C0OX)
MENTHOL (UNII: L7T10EIP3A)
WATER (UNII: 059QF0KO0R)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
SORBITOL SOLUTION (UNII: 8KW3E207O2)

Product Characteristics
Color	white (colorless)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71399-1005-4	118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/11/2022	01/17/2024
2	NDC: 71399-1005-8	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/11/2022	01/17/2024
3	NDC: 71399-1005-6	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/11/2022	01/17/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M012	11/11/2022	01/17/2024

Labeler - Akron Pharma Inc. (067878881)

Registrant - SLV PHARMACEUTICALS LLC (081225162)

Establishment
Name	Address	ID/FEI	Business Operations
SLV PHARMACEUTICALS LLC		081225162	manufacture(71399-1005)

Revised: 1/2024

Document Id: 77a8f91c-a576-4b5d-abcb-bfee6cbf048d

34390-5

Set id: 8a650a18-6738-4910-a663-731cc2cc93a1

Version: 2

Effective Time: 20240118