NDC 52471-111

Sorbitol

Sorbitol

Sorbitol is a Rectal Solution in the Human Otc Drug category. It is labeled and distributed by H&h Laboratories, Inc.. The primary component is Sorbitol.

• Product ID: 52471-111_f251e7d4-222e-4e0f-9317-2e75bdaa86f2
• NDC: 52471-111
• Product Type: Human Otc Drug
• Proprietary Name: Sorbitol
• Generic Name: Sorbitol
• Dosage Form: Solution
• Route of Administration: RECTAL
• Marketing Start Date: 2013-06-10
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part334
• Labeler Name: H&H Laboratories, Inc.
• Substance Name: SORBITOL
• Active Ingredient Strength: 1 g/mL
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 52471-111-16

473 mL in 1 BOTTLE (52471-111-16)

• Marketing Start Date: 2013-06-10
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 52471-111-16 [52471011116]

Sorbitol SOLUTION

• Marketing Category: OTC monograph not final
• Application Number: part334
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2013-06-10
• Inactivation Date: 2019-11-27

Drug Details

Active Ingredients

Ingredient	Strength
SORBITOL	1 g/mL

OpenFDA Data

• SPL SET ID: debf8549-7369-40e7-a594-bff433a7bbf0
• Manufacturer:
  • H&H Laboratories, Inc.
• UNII:
  • 506T60A25R

NDC Crossover Matching brand name "Sorbitol" or generic name "Sorbitol"

NDC	Brand Name	Generic Name
0264-2301	Sorbitol	Sorbitol
0338-0295	Sorbitol	Sorbitol
52471-111	Sorbitol	Sorbitol
54162-700	Sorbitol	Sorbitol
57896-435	SORBITOL	sorbitol
57896-758	GeriCare Sorbitol Solution	Sorbitol