HUMCO DEWEES CARMINATIVE- magnesium carbonate suspension

Humco Dewees Carminative by

Drug Labeling and Warnings

Humco Dewees Carminative by is a Otc medication manufactured, distributed, or labeled by Humco Holding Group, inc., Pharma Nobis, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

Magnesium Carbonate 250 mg per tsp. (5 mL)

Purpose

Carminative

Use

For the temporary relief of upset stomach or sour stomach, and acid indigestion.

Warnings

Do not use if you have kidney desease.

When sing this product

Do not take more than the maximum recommended daily dose (Adults 8 tsps. - children 4 tsps.), or use the maximum dosage of this product for more than 2 weeks, except under the advice and supervision of a doctor.

May have laxative effect.

Ask a doctor before use

If you are taking prescription drugs. Antacids may interact with certain prescription drugs.

Keep out of reach of children.

In the case of accidental overdose, seek professional assistance or contact a Poison Control center immediately.

Directions

(Shake well before using)

Follow dosage below or as directed by a doctor.

Adults and children 12 yrs. and older: 2 tsps. every 3 to 4 hrs.

Children 6 to 12 yrs. of age: 1 tsp. every 3 to 4 hrs.

Children under 2 yrs. of age: consult a doctor before use.

Inactive ingredients

Asafetida, Avicel, Benzyl Alcohol, Carrageenan, Glycerin, Purified Water, Simethicone, Sucrose, Xanthan Gum

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INGREDIENTS AND APPEARANCE

HUMCO DEWEES CARMINATIVE 
magnesium carbonate suspension

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0395-0713
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MAGNESIUM CARBONATE (UNII: 0E53J927NA) (CARBONATE ION - UNII:7UJQ5OPE7D)	MAGNESIUM CARBONATE	50 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
CARRAGEENAN (UNII: 5C69YCD2YJ)
DIMETHICONOL/TRIMETHYLSILOXYSILICATE CROSSPOLYMER (40/60 W/W; 1000000 PA.S) (UNII: 83D19O7250)
BENZYL ALCOHOL (UNII: LKG8494WBH)
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
ASAFETIDA (UNII: W9FZA51AS1)
GLYCERIN (UNII: PDC6A3C0OX)
SUCROSE (UNII: C151H8M554)
WATER (UNII: 059QF0KO0R)
XANTHAN GUM (UNII: TTV12P4NEE)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0395-0713-92	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/13/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part331	03/25/1998

Labeler - Humco Holding Group, inc. (825672884)

Registrant - Humco Holding Group, inc. (825672884)

Establishment
Name	Address	ID/FEI	Business Operations
Humco Holding group, Inc.		825672884	manufacture(0395-0713) , analysis(0395-0713) , pack(0395-0713) , label(0395-0713)