Sorbitol

Product NDC
52471-111
11-digit product format
524710111
Labeler code
52471
Product ID
52471-111_f251e7d4-222e-4e0f-9317-2e75bdaa86f2
Type
HUMAN OTC DRUG
Nonproprietary name
Sorbitol
Dosage form
SOLUTION
Route
RECTAL
Labeler
H&H Laboratories, Inc.
Application
part334
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2013-06-10
Marketing end
0000-00-00
Substance
SORBITOL
Active strength
1 g/mL
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
52471-111-162019-11-27C16284748780-19855d018-e0b7-cd31-e053-dbdaa90ab51aDRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52471-111-16Sorbitol473 mL in 1 BOTTLESOLUTION4731

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
SORBITOLACTIVE INGREDIENT506T60A25RSORBITOL SOLUTION [H&H LABORATORIES, INC.]1
SORBITOLACTIVE MOIETY506T60A25RSORBITOL SOLUTION [H&H LABORATORIES, INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RSORBITOL SOLUTION [H&H LABORATORIES, INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52471-111SORBITOL SOLUTION [H&H LABORATORIES, INC.]1Legacy NDC, 1 package rows20130611_debf8549-7369-40e7-a594-bff433a7bbf0.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
52471-111-1652471011116473 mL in 1 BOTTLE473 mlHistorical