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NDC 11788-0021-03 D-Cal Kids 750 mg/1 Details

D-Cal Kids 750 mg/1

D-Cal Kids is a ORAL TABLET, CHEWABLE in the HUMAN OTC DRUG category. It is labeled and distributed by AiPing Pharmaceutical, Inc.. The primary component is CALCIUM CARBONATE.

MedlinePlus Drug Summary

Calcium carbonate is a dietary supplement used when the amount of calcium taken in the diet is not enough. Calcium is needed by the body for healthy bones, muscles, nervous system, and heart. Calcium carbonate also is used as an antacid to relieve heartburn, acid indigestion, and upset stomach. It is available with or without a prescription. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.

Related Packages: 11788-0021-03
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Calcium Carbonate

Product Information

NDC	11788-0021
Product ID	11788-021_e768b861-1993-1281-e053-2a95a90a64ac
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	D-Cal Kids
Proprietary Name Suffix	n/a
Non-Proprietary Name	Calcium Carbonate
Product Type	HUMAN OTC DRUG
Dosage Form	TABLET, CHEWABLE
Route	ORAL
Active Ingredient Strength	750
Active Ingredient Units	mg/1
Substance Name	CALCIUM CARBONATE
Labeler Name	AiPing Pharmaceutical, Inc.
Pharmaceutical Class	Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE]
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH FINAL
Application Number	part331
Listing Certified Through	2023-12-31

Package

Package Images

NDC 11788-0021-03 (11788002103)

Pricing Information	N/A
NDC Package Code	11788-021-03
Billing NDC	11788002103
Package	30 TABLET, CHEWABLE in 1 BOTTLE (11788-021-03)
Marketing Start Date	1997-09-17
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL e768b861-1992-1281-e053-2a95a90a64ac Details

ACTIVE INGREDIENTS

Calcium Carbonate 750 mg

PURPOSES

Antacid

USES

Relieves

heartburn
acid indigestion
sour stomach
upset stomach due to these symptoms

WARNINGS

Ask a doctor or pharmacist before use if you are taking a prescription drug. Antacids may interact with certain prescription drugs. When using this product do not take more than 5 tablets in a 24 hour period. Keep out of reach of children.

Keep out of reach of children

Directions

chew one tablet daily. If symptoms persist, ask a doctor.

Other Information

store in a dry place
do not use if imprinted seal under cap is torn or open

Inactive ingredients

cholecalciferol, aspartame, citric acid, D&C Yellow #6, FD&C Blue #1, FD&C Red #40, FD&C Yellow #5, FD&C Yellow #10, flavors, magnesium stearate, sorbitol

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

D-CAL KIDS

calcium carbonate tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:11788-021
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB, CARBONATE ION - UNII:7UJQ5OPE7D)	CALCIUM CARBONATE	750 mg

Ingredient Name	Strength
Inactive Ingredients
CHOLECALCIFEROL (UNII: 1C6V77QF41)
ASPARTAME (UNII: Z0H242BBR1)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C RED NO. 40 (UNII: WZB9127XOA)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
MAGNESIUM STEARATE (UNII: 70097M6I30)
SORBITOL (UNII: 506T60A25R)

Product Characteristics
Color	orange	Score	no score
Shape	FREEFORM	Size	17mm
Flavor		Imprint Code	0
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:11788-021-03	30 in 1 BOTTLE; Type 0: Not a Combination Product	09/17/1997

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part331	09/17/1997

Labeler - AiPing Pharmaceutical, Inc. (079674526)

Registrant - AiPing Pharmaceutical, Inc. (079674526)

Name	Address	ID/FEI	Business Operations
Establishment
A&Z Pharmaceutical, Inc.		080225262	manufacture(11788-021)

Revised: 8/2022

Document Id: e768b861-1993-1281-e053-2a95a90a64ac

Set id: e768b861-1992-1281-e053-2a95a90a64ac

Version: 1

Effective Time: 20220829