PEPCID AC ORIGINAL STRENGTH- famotidine tablet, film coated 
Johnson & Johnson Consumer Inc.

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Pepcid AC

Original Strength

Drug Facts

Active ingredient (in each tablet)

Famotidine 10 mg

Purpose

Acid reducer

Uses

Warnings

Allergy alert

Do not use if you are allergic to famotidine or other acid reducers

Do not use

  • if you have trouble or pain swallowing food, vomiting with blood, or bloody or black stools. These may be signs of a serious condition. See your doctor.
  • with other acid reducers

Ask a doctor before use if you have

  • had heartburn over 3 months. This may be a sign of a more serious condition.
  • heartburn with lightheadedness, sweating, or dizziness
  • chest pain or shoulder pain with shortness of breath; sweating; pain spreading to arms, neck or shoulders; or lightheadedness
  • frequent chest pain
  • frequent wheezing, particularly with heartburn
  • unexplained weight loss
  • nausea or vomiting
  • stomach pain
  • kidney disease

Ask a doctor or pharmacist before use if you are taking a prescription drug. Acid reducers may interact with certain prescription drugs.

Stop use and ask a doctor if

  • your heartburn continues or worsens
  • you need to take this product for more than 14 days

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. (1-800-222-1222)

Directions

Other information

Inactive ingredients

carnauba wax, hydroxypropyl cellulose, hypromellose, magnesium stearate, microcrystalline cellulose, pregelatinized starch, red iron oxide, talc, titanium dioxide

Questions or comments?

1-800-755-4008 (toll-free) or 215-273-8755 (collect)

PRINCIPAL DISPLAY PANEL

NDC 16837-872-20

ORIGINAL STRENGTH

Pepcid ®

AC

Famotidine Tablets 10 mg

Acid Reducer

Just One Tablet!

Prevents & Relieves Heartburn

Due to Acid Indigestion

actual size

30 Tablets

Principal Display Panel

PEPCID AC  ORIGINAL STRENGTH
famotidine tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:16837-872
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
FAMOTIDINE (UNII: 5QZO15J2Z8) (FAMOTIDINE - UNII:5QZO15J2Z8) FAMOTIDINE10 mg
Inactive Ingredients
Ingredient NameStrength
CARNAUBA WAX (UNII: R12CBM0EIZ)  
HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
TALC (UNII: 7SEV7J4R1U)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
Product Characteristics
Colorpink (pale rose) Scoreno score
ShapeSQUARE (rounded edges) Size7mm
FlavorImprint Code PEPCID;AC
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:16837-872-101 in 1 CARTON01/21/201112/31/2023
110 in 1 BLISTER PACK; Type 0: Not a Combination Product
2NDC:16837-872-303 in 1 CARTON10/01/1995
210 in 1 BLISTER PACK; Type 0: Not a Combination Product
3NDC:16837-872-314 in 1 CARTON10/01/199512/31/2023
310 in 1 BLISTER PACK; Type 0: Not a Combination Product
4NDC:16837-872-601 in 1 CARTON10/01/1995
460 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
5NDC:16837-872-901 in 1 CARTON10/01/1995
590 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
6NDC:16837-872-203 in 1 CARTON01/21/2011
610 in 1 BLISTER PACK; Type 0: Not a Combination Product
7NDC:16837-872-221 in 1 CARTON01/21/2011
790 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
8NDC:16837-872-751 in 1 CARTON03/15/202108/31/2024
875 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NDANDA02032510/01/1995
Labeler - Johnson & Johnson Consumer Inc. (878046358)

Revised: 3/2024
Document Id: 1385f25e-07c8-2400-e063-6394a90a2787
Set id: 54f4086f-e443-4e7e-8c7e-94e152e1c256
Version: 18
Effective Time: 20240313
 
Johnson & Johnson Consumer Inc.