EQUALINE EXTRA STRENGTH ASSORTED BERRY ANTACID- calcium carbonate tablet, chewable

Equaline Extra Strength Assorted Berry Antacid by

Drug Labeling and Warnings

Equaline Extra Strength Assorted Berry Antacid by is a Otc medication manufactured, distributed, or labeled by UNITED NATURAL FOODS, INC. DBA UNFI, Guardian Drug Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT (in each tablet)

Calcium carbonate 750 mg

PURPOSE

Antacid

USE(S)

relieves:

• acid indigestion
• heartburn

WARNINGS

.

ASK A DOCTOR OR PHARMACIST BEFORE USE IF YOU ARE

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

WHEN USING THIS PRODUCT

do not take more than 10 tablets 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.

IF PREGNANT OR/BREASTFEEDING,

ask a health professional before use.

KEEP OUT OF REACH OF CHILDREN

.

DIRECTIONS

• adults and children 12 years of age and over: chew 2-4 tablets as symptoms occur, or as directed by a doctor.

OTHER INFORMATION

• each tablet contains: elemental calcium 300 mg,
• do not use if printed seal under cap is torn or missing. 
• store at room temperature. Keep the container tightly closed..

INACTIVE INGREDIENTS

adipic acid, corn starch, crospovidone, dextrose, FD&C blue 1 lake, FD&C red 40 lake, flavors, magnesium stearate, maltodextrin, sucrose, talc.

PRINCIPAL DISPLAY PANEL

NDC: 41163-129-66

EQUALINE

compare to TUMS® Extra Strength 750 active ingredient*   

extra strength
antacid tablets

calcium carbonate 750mg

relieves

heartburn and

acid indigestion

assorted berry flavors

200 CHEWABLE TABLETS

NDC: 41163-129-22

EQUALINE

compare to TUMS® Extra Strength 750 active ingredient*   

extra strength
antacid tablets

calcium carbonate 750mg

relieves

heartburn and

acid indigestion

assorted berry flavors

96 CHEWABLE TABLETS

INGREDIENTS AND APPEARANCE

EQUALINE EXTRA STRENGTH ASSORTED BERRY ANTACID 
calcium carbonate tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 41163-129
Route of Administration	ORAL

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

Inactive Ingredients
Ingredient Name	Strength
STARCH, CORN (UNII: O8232NY3SJ)
DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
SUCROSE (UNII: C151H8M554)
TALC (UNII: 7SEV7J4R1U)
CROSPOVIDONE (UNII: 68401960MK)
ADIPIC ACID (UNII: 76A0JE0FKJ)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C RED NO. 40 (UNII: WZB9127XOA)

Product Characteristics
Color	RED, PINK, BLUE	Score	no score
Shape	ROUND	Size	16mm
Flavor	BERRY (Raspberry, Strawberry, Wild berry)	Imprint Code	G127
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 41163-129-66	200 in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2024
2	NDC: 41163-129-22	96 in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	part331	05/01/2024

Labeler - UNITED NATURAL FOODS, INC. DBA UNFI (943556183)

Establishment
Name	Address	ID/FEI	Business Operations
Guardian Drug Company		119210276	MANUFACTURE(41163-129)