Home NDC 0135-0090 CITRUCEL
Product NDC 0135-0090
11-digit product format 001350090
Labeler code 0135
Product ID 0135-0090_4d50ac6b-2405-defb-e063-6394a90aa71c
Type HUMAN OTC DRUG
Nonproprietary name methylcellulose
Dosage form POWDER, FOR SOLUTION
Route ORAL
Labeler Haleon US Holdings LLC
Application M007
Marketing category OTC MONOGRAPH DRUG
Marketing start 2010-09-16
Substance METHYLCELLULOSE (4000 MPA.S)
Active strength 2 g/10.2g
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base CITRUCEL
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength METHYLCELLULOSE (4000 MPA.S) 2 g/10.2g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination MRJ667KA5E Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1868843 Internal RxNorm lookup 1868847 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0135-0090-70 CITRUCEL 479 g in 1 BOTTLE POWDER, FOR SOLUTION 479 17 0135-0090-74 CITRUCEL 907 g in 1 BOTTLE POWDER, FOR SOLUTION 907 17 0135-0090-75 CITRUCEL 1191 g in 1 BOTTLE POWDER, FOR SOLUTION 1191 17
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded METHYLCELLULOSE (4000 MPA.S) ACTIVE INGREDIENT MRJ667KA5E CITRUCEL (METHYLCELLULOSE) POWDER, FOR SOLUTION [GLAXOSMITHKLINE CONSUMER HEALTHCARE LP] 6 METHYLCELLULOSE (4000 MPA.S) ACTIVE MOIETY MRJ667KA5E CITRUCEL (METHYLCELLULOSE) POWDER, FOR SOLUTION [GLAXOSMITHKLINE CONSUMER HEALTHCARE LP] 6 ASPARTAME INACTIVE INGREDIENT Z0H242BBR1 CITRUCEL (METHYLCELLULOSE) POWDER, FOR SOLUTION [GLAXOSMITHKLINE CONSUMER HEALTHCARE LP] 6 CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS INACTIVE INGREDIENT L11K75P92J CITRUCEL (METHYLCELLULOSE) POWDER, FOR SOLUTION [GLAXOSMITHKLINE CONSUMER HEALTHCARE LP] 6 CITRIC ACID MONOHYDRATE INACTIVE INGREDIENT 2968PHW8QP CITRUCEL (METHYLCELLULOSE) POWDER, FOR SOLUTION [GLAXOSMITHKLINE CONSUMER HEALTHCARE LP] 6 FD&C YELLOW NO. 6 INACTIVE INGREDIENT H77VEI93A8 CITRUCEL (METHYLCELLULOSE) POWDER, FOR SOLUTION [GLAXOSMITHKLINE CONSUMER HEALTHCARE LP] 6 MALIC ACID INACTIVE INGREDIENT 817L1N4CKP CITRUCEL (METHYLCELLULOSE) POWDER, FOR SOLUTION [GLAXOSMITHKLINE CONSUMER HEALTHCARE LP] 6 MALTODEXTRIN INACTIVE INGREDIENT 7CVR7L4A2D CITRUCEL (METHYLCELLULOSE) POWDER, FOR SOLUTION [GLAXOSMITHKLINE CONSUMER HEALTHCARE LP] 6 POTASSIUM CITRATE INACTIVE INGREDIENT EE90ONI6FF CITRUCEL (METHYLCELLULOSE) POWDER, FOR SOLUTION [GLAXOSMITHKLINE CONSUMER HEALTHCARE LP] 6 RIBOFLAVIN INACTIVE INGREDIENT TLM2976OFR CITRUCEL (METHYLCELLULOSE) POWDER, FOR SOLUTION [GLAXOSMITHKLINE CONSUMER HEALTHCARE LP] 6 SUCROSE INACTIVE INGREDIENT C151H8M554 CITRUCEL (METHYLCELLULOSE) POWDER, FOR SOLUTION [GLAXOSMITHKLINE CONSUMER HEALTHCARE LP] 6 TITANIUM DIOXIDE INACTIVE INGREDIENT 15FIX9V2JP CITRUCEL (METHYLCELLULOSE) POWDER, FOR SOLUTION [GLAXOSMITHKLINE CONSUMER HEALTHCARE LP] 6 TRICALCIUM PHOSPHATE INACTIVE INGREDIENT K4C08XP666 CITRUCEL (METHYLCELLULOSE) POWDER, FOR SOLUTION [GLAXOSMITHKLINE CONSUMER HEALTHCARE LP] 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0135-0090 CITRUCEL (METHYLCELLULOSE) POWDER, FOR SOLUTION [HALEON US HOLDINGS LLC] 16 Current NDC, Legacy NDC, 3 package rows 20240612_9d5f2244-a610-4d45-b6e8-e79bb17a558f.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 30 of 42 · 833 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 0135-0090-70 00135009070 479 g in 1 BOTTLE (0135-0090-70) 479 g 2010-09-16 0000-00-00 No No Current 0135-0090-74 00135009074 907 g in 1 BOTTLE (0135-0090-74) 907 g 2010-09-16 0000-00-00 No No Current 0135-0090-75 00135009075 1191 g in 1 BOTTLE (0135-0090-75) 1191 g 2010-09-16 0000-00-00 No No Current