HUMCO DEWEES CARMINATIVE- magnesium carbonate suspension 
Humco Holding Group, inc.

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Humco Dewee's Carminative

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 under 12 yrs. of age: consult a doctor before use.

Inactive ingredients

Alcohol 5%, Asafetida, Avicel, Benzyl Alcohol, Carrageenan, Glycerin, Microcrystalline Cellulose and Carboxymethylcelloulose Sodium, Purified Water, Simethicone, Sucrose, Xanthan Gum

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HUMCO DEWEES CARMINATIVE 
magnesium carbonate suspension
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0395-0713
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MAGNESIUM CARBONATE (UNII: 0E53J927NA) (CARBONATE ION - UNII:7UJQ5OPE7D) MAGNESIUM CARBONATE50 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0395-0713-9259 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/13/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00103/25/1998
Labeler - Humco Holding Group, inc. (825672884)
Registrant - Pharma Nobis, LLC (118564114)
Establishment
NameAddressID/FEIBusiness Operations
Pharma Nobis, LLC118564114manufacture(0395-0713) , analysis(0395-0713) , pack(0395-0713) , label(0395-0713)

Revised: 12/2023
Document Id: 0c92d0b3-1768-de2d-e063-6394a90a34d1
Set id: 163bceeb-ca74-413e-88b9-5c7bc9bbeb0d
Version: 6
Effective Time: 20231215
 
Humco Holding Group, inc.