REGULAR STRENGTH ASSORTED FLAVORS- antacid calcium carbonate tablet, chewable

Regular Strength by

Drug Labeling and Warnings

Regular Strength by is a Otc medication manufactured, distributed, or labeled by AKRON PHARMA INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Calcium Carbonate USP 500mg

Purpose

Antacid

Uses

relieves:

heartburn

sour stomach

acid indigestion

upset stomach associated with these symptoms

Warnings

Ask a doctor or pharmacist before use if you are presentlytaking a prescription drug. Antacids may interact with certain prescription drugs.

When using this product

• do not take more than 15 tablets in 24 hours
• If pregnant do not take more than 10 tablets in 24 hours
• do not use the maximum dosage for more than 2 weeks except under the advice and supervision of a doctor.

KEEP OUT OF REACH OF CHILDREN

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.
• Do not swallow tablets whole,
• Do not take for symptoms that persist for more than 2 weeks unless advised by a doctor.

Other Information

• Each tablet contains: elemental calcium 200 mg
• Store at room temperature. Keep the container tightly closed

Safety sealed: Do not use if printed seal under cap is torn or missing.

Inactive ingredients

adipic acid, D&C Red No.27 lake, D&C Yellow No.10 lake, dextrose, FD&C Blue No.1 lake, FD&C Yellow No.6 lake, flavors, magnesium stearate, maltodextrin, starch, sucralose.

QUESTIONS

Questions or comments? call toll-free 1-877-225-6999

Manufactured for:

Akron Pharma Inc.,

Fairfield, NJ-07004

www.akronpharma.com

*This product is not manufactured or distributed by GlaxoSmithKline LLC, owner of the registered trademark, Regular Strength Tums®.

Package/Label Principal Display Panel

INGREDIENTS AND APPEARANCE

REGULAR STRENGTH  ASSORTED FLAVORS
antacid calcium carbonate tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71399-9939
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB)	CALCIUM CARBONATE	500 mg

Inactive Ingredients
Ingredient Name	Strength
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
STARCH, CORN (UNII: O8232NY3SJ)
SUCRALOSE (UNII: 96K6UQ3ZD4)
ADIPIC ACID (UNII: 76A0JE0FKJ)
D&C RED NO. 27 (UNII: 2LRS185U6K)

Product Characteristics
Color	white	Score	no score
Shape	ROUND	Size	16mm
Flavor	FRUIT	Imprint Code	AP101
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71399-9939-1	150 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/23/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M001	09/23/2025

Labeler - AKRON PHARMA INC (067878881)