63868-565 : Heartburn Relief Oral Suspension


NDC63868-565
Labeler: Chain Drug Marketing Association
Product Type: Human OTC Drug
Drug Name:  Heartburn Relief
Dosage Form: Oral Suspension
Application #: part331
Rev. Date: 


NDC Package Codes:

  • 63868-565-12: 355 ML IN 1 BOTTLE (63868‑565‑12)

Active Ingredients:

  • Aluminum Hydroxide
  • Magnesium Carbonate

Dosage Strength:

  • 254 mg/5mL
  • 237.5 mg/5mL

Related Products:

Based on records with the same trade name.
  • 17312-030 Heartburn Relief Oral Tablet, Orally Disintegrating by Trp Company
  • 30142-047 Ranitidine 150 mg (As Ranitidine Hydrochloride 168 mg) Oral Tablet by Kroger Company
  • 30142-271 Ranitidine 75 mg (As Ranitidine Hydrochloride 84 mg) Oral Tablet by Kroger Company
  • 30142-852 Heartburn Relief (Ranitidine 150 mg) by Kroger Company
  • 30142-950 Ranitidine 150 mg (As Ranitidine Hydrochloride 168 mg) Oral Tablet by Kroger Company
  • 37808-852 Ranitidine 150 mg (As Ranitidine Hydrochloride 168 mg) Oral Tablet by H E B
  • 37808-950 Ranitidine 150 mg (As Ranitidine Hydrochloride 168 mg) Oral Tablet by H E B
  • 41163-619 Heartburn Relief 75 mg/1 Oral Tablet by Supervalu Inc.
  • 41250-022 Cimetidine 200 mg Oral Tablet by Meijer Distribution Inc
  • 41250-493 Heartburn Relief 10 mg Oral Tablet, Film Coated by Meijer Distribution Inc
  • 41250-712 Heartburn Relief 20 mg Oral Tablet, Film Coated by Meijer Distribution Inc
  • 52904-448 Heartburn Relief 10 mg/1 Oral Tablet by Select Corporation
  • 55319-022 Cimetidine 200 mg Oral Tablet by Family Dollar Services Inc
  • 56062-099 Heartburn Relief 150 mg Oral Tablet, Film Coated by Publix Super Markets Inc
  • 57955-0022 Heartburn Relief Oral Liquid by King Bio Inc.
  • 57955-5022 Heartburn Relief Oral Liquid by King Bio Inc.
  • 59262-605 Heartburn Relief Oral Tablet, Orally Disintegrating by Similasan Corporation
  • 59779-022 Cimetidine 200 mg Oral Tablet by Cvs Pharmacy
  • 71713-701 Heartburn Relief 20 mg Oral Tablet, Film Coated by Thirty Madison Inc
  • 83059-0005 Heartburn Relief 10 mg Oral Tablet, Film Coated by Shield Pharmaceuticals Corp

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.