NDC 0283-0808

CEO-TWO

Laxative

CEO-TWO is a Rectal Suppository in the Human Otc Drug category. It is labeled and distributed by Beutlich Pharmaceuticals, Llc. The primary component is Potassium Bitartrate; Sodium Bicarbonate.

• Product ID: 0283-0808_6c8d74eb-b989-47dd-a528-5a686d85f700
• NDC: 0283-0808
• Product Type: Human Otc Drug
• Proprietary Name: CEO-TWO
• Generic Name: Laxative
• Dosage Form: Suppository
• Route of Administration: RECTAL
• Marketing Start Date: 2008-08-15
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part334
• Labeler Name: Beutlich Pharmaceuticals, LLC
• Substance Name: POTASSIUM BITARTRATE; SODIUM BICARBONATE
• Active Ingredient Strength: 927 mg/3.7g; mg/3.7g
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 0283-0808-12

12 BOX in 1 BOX (0283-0808-12) > 6 BOX in 1 BOX (0283-0808-36) > 2 DOSE PACK in 1 BOX (0283-0808-11) > 3.7 g in 1 DOSE PACK (0283-0808-00)

• Marketing Start Date: 2008-08-15
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0283-0808-36 [00283080836]

CEO-TWO SUPPOSITORY

• Marketing Category: OTC monograph not final
• Application Number: part334
• Product Type: HUMAN OTC DRUG
• Billing Unit: EA
• Marketing Start Date: 2008-08-15

NDC 0283-0808-00 [00283080800]

CEO-TWO SUPPOSITORY

• Marketing Category: OTC monograph not final
• Application Number: part334
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2008-08-15

NDC 0283-0808-12 [00283080812]

CEO-TWO SUPPOSITORY

• Marketing Category: OTC monograph not final
• Application Number: part334
• Product Type: HUMAN OTC DRUG
• Billing Unit: EA
• Marketing Start Date: 2008-08-15

NDC 0283-0808-54 [00283080854]

CEO-TWO SUPPOSITORY

• Marketing Category: OTC monograph not final
• Application Number: part334
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2008-08-15

NDC 0283-0808-11 [00283080811]

CEO-TWO SUPPOSITORY

• Marketing Category: OTC monograph not final
• Application Number: part334
• Product Type: HUMAN OTC DRUG
• Billing Unit: EA
• Marketing Start Date: 2008-08-15

Drug Details

Active Ingredients

Ingredient	Strength
POTASSIUM BITARTRATE	927 mg/3.7g

OpenFDA Data

• SPL SET ID: d868de56-ac3b-4e44-8aa5-031661f0ac25
• Manufacturer:
  • Beutlich Pharmaceuticals, LLC
• UNII:
  • 8MDF5V39QO
  • NPT6P8P3UU
• RxNorm Concept Unique ID - RxCUI:
  • 636188
  • 636185
• UPC Code:
  • 0723797808542