0132-0195 : Pedia-lax 2.8 g/4ml Rectal Liquid


NDC: 0132-0195
Labeler: C.b. Fleet Company, Inc.
Product Type: Human OTC Drug
Drug Name:  Pedia-lax
Dosage Form: Rectal Liquid
Application #: part334
Rev. Date: 


NDC Package Codes:

  • 0132-0195-12: 6 APPLICATOR IN 1 CARTON (0132‑0195‑12) > 4 ML IN 1 APPLICATOR

Active Ingredients:

  • Glycerin

Dosage Strength:

  • 2.8 g/4mL

Pharmaceutical Classes:

  • Allergens [CS]
  • Cell-mediated Immunity [PE]
  • Glycerol [CS]
  • Increased Histamine Release [PE]
  • Increased IgG Production [PE]
  • Non-Standardized Chemical Allergen [EPC]

Related Products:

Based on records with the same trade name.
  • 0132-0081 Pedia-lax 1 g/1 Rectal Suppository by C.b. Fleet Company, Inc.
  • 0132-0106 Pedia-lax 50 mg/118ml Oral Liquid by C.b. Fleet Company, Inc.
  • 0132-0107 Pedia-lax 50 mg/15ml Oral Liquid by C.b. Fleet Company, Inc.
  • 0132-0190 Pedia-lax 2.8 g/1 Rectal Liquid by C.b. Fleet Company, Inc.
  • 0132-0202 Pedia-lax Rectal Enema by C.b. Fleet Company, Inc.
  • 0132-0655 Pedia-lax Chewable 400 mg Chewable Tablet by C.b. Fleet Company, Inc.

NDC QR Code

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NDC 0132-0195 QR Code

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Related Discussions:

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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.