Pays: États-Unis
Langue: anglais
Source: NLM (National Library of Medicine)
CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB)
Humco Holding Group, Inc.
CALCIUM CARBONATE
CALCIUM CATION 1 g in 1 g
ORAL
OTC DRUG
Antacid For relief of heartburn, acid ingestion, and upset stomach associated with these symptoms. if you are preganant or nursing a baby.
OTC monograph final
CALCIUM CARBONATE- CALCIUM CARBONATE POWDER HUMCO HOLDING GROUP, INC. ---------- HUMCO CALCIUM CARBONATE, USP Drug Facts ACTIVE INGREDIENT Calcium Carbonate PURPOSE Antacid USE For relief of heartburn, acid ingestion, and upset stomach associated with these symptoms. WARNINGS Except under the supervision of a doctor: do not administer to children under 6 years of age. do not take more than 3 teaspoonfuls in a 24 hour period. do not use the maximum dosge of this product for more than 2 weeks except under the advice and supervision of a doctor or other health professional. ASK A DOCTOR BEFORE USE if you are preganant or nursing a baby. KEEP OUT OF REACH OF CHILDREN. In case of accidental overdose, seek professional assistance or contact a Poison Control immediately. DIRECTIONS Adults and children 6 yrs. of age and older: Take 1/2 level tsp. in 1/2 glass (4 fl oz) of water every 2 hrs. up to maximum dosage or as directed by a doctor. INACTIVE INGREDIENTS None PRINCIPAL DISPLAY PANEL CALCIUM CARBONATE calcium carbonate powder PRODUCT INFORMATION PRODUCT TYPE HUMAN OTC DRUG ITEM CODE (SOURCE) NDC:0395-0431 ROUTE OF ADMINISTRATION ORAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRENGTH CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6Z B) CALCIUM CATION 1 g in 1 g INACTIVE INGREDIENTS INGREDIENT NAME STRENGTH WATER (UNII: 059QF0KO0R) PACKAGING # ITEM CODE PACKAGE DESCRIPTION MARKETING START DATE MARKETING END DATE 1 NDC:0395- 0431-01 454 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/13/2017 Humco Holding Group, Inc. MARKETING INFORMATION MARKETING CATEGORY APPLICATION NUMBER OR MONOGRAPH CITATION MARKETING START DATE MARKETING END DATE OTC Monograph Drug M001 01/01/2008 LABELER - Humco Holding Group, Inc. (825672884) REGISTRANT - Pharma Nobis, LLC (118564114) ESTABLISHMENT NAME ADDRESS ID/FEI BUSINESS OPERATIONS Pharma Nobis, LLC 118564114 manufacture(0395-0431) , analysis(0395-0431) , pack(0395-0431) , label(0395-0431) Revised: 12/2023 Lire le document complet