CHILDRENS ANTACID- calcium carbonate liquid

Childrens Antacid by

Drug Labeling and Warnings

Childrens Antacid by is a Otc medication manufactured, distributed, or labeled by CVS, Guardian Drug Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT (in each 5 mL)

Calcium carbonate 400 mg

PURPOSE

Antacid

USE(S)

relieves:

• acid indigestion
• heartburn
• sour stomach
• upset stomach associated with these symptoms

WARNINGS

Do  not take nore than 15 mL (age 2-5 yrs) or 30 mL (age 6-11 yrs) in a 24-hour period, or use the maximum dosage of this product for more than 2 weeks, except under the advice and supervision of a doctor.

ASK A DOCTOR OR PHARMACIST BEFORE USE IF THE CHILD IS

• presently taking a prescription drug. Antacids may interact with certain prescription drugs.

STOP USE AND ASK DOCTOR IF

symptoms lasts more than two weeks

KEEP THIS AND ALL DRUGS OUT OF REACH OF CHILDREN

.

DIRECTIONS

• shake well before use
• find the right dose on the chart below based on weight (preferred), otherwise use age.
• repeat dose as needed
• dosing cup provided
• mL=milliliter

Dosing Chart

Weight (lbs.)	Age	Dose
under 24	under 2 yrs.	ask a doctor
24-47	2-5 yrs.	5 mL
48-95	6-11 yrs.	10 mL

OTHER INFORMATION

• each 5 mL contains: calcium 161 mg
• store at controlled room temperature 20-25ºC (68ºF-77ºF)

INACTIVE INGREDIENTS

benzyl alcohol, D&C yellow#10 dye, FD&C red#40 dye, flavors, glycerin, hydroxyethyl cellulose, methylparaben, propylene glycol, propylparaben, purified water, sodium citrate, sorbitol, sucralose, xanthan gum.

PRINCIPAL DISPLAY PANEL

CVS

Health.

Compare to the active ingredient in pepto® kids*

Orange Cream
NDC: 51316-657-03
Children's 
Antacid Liquid

CALCIUM CARBONATE 400 mg

RELIEVES :

• Acid indigestion & heartburn
• Sour & upset Stomach due to these symptoms

Orange Cream 
4 FL OZ  (118 mL)

INGREDIENTS AND APPEARANCE

CHILDRENS ANTACID 
calcium carbonate liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51316-657
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB)	CALCIUM CARBONATE	400 mg  in 5 mL

Inactive Ingredients
Ingredient Name	Strength
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
BENZYL ALCOHOL (UNII: LKG8494WBH)
FD&C RED NO. 40 (UNII: WZB9127XOA)
GLYCERIN (UNII: PDC6A3C0OX)
HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) (UNII: S38J6RZN16)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
SORBITOL (UNII: 506T60A25R)
SUCRALOSE (UNII: 96K6UQ3ZD4)
XANTHAN GUM (UNII: TTV12P4NEE)

Product Characteristics
Color	ORANGE	Score
Shape		Size
Flavor	ORANGE	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51316-657-03	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/15/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M001	01/15/2025

Labeler - CVS (062312574)

Establishment
Name	Address	ID/FEI	Business Operations
Guardian Drug Company		119210276	MANUFACTURE(51316-657)