Home NDC 11822-1015-01 NDC 11822-1015-01 - Rite Aid Hot and Cold Roll On This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
Product NDC 11822-1015
Requested NDC 11822-1015-01
Package NDCs from labels 11822-1015-1, 11822-1015-01
Manufacturer Rite Aid | Derma Care Research Labs, LLC
Effective date 2024-12-15
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 11822-1015-1 Rite Aid Hot and Cold Roll On 71 g in 1 BOTTLE, PLASTIC LIQUID 71 2 11822-1015-1 Rite Aid Hot and Cold Roll On 1 in 1 CARTON LIQUID 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 11822-1015 RITE AID HOT AND COLD ROLL ON (MENTHOL 16%) LIQUID [RITE AID] 2 Current NDC, 2 package rows 20241217_fc4b2635-280b-267f-e053-6294a90a5e22.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 31 of 363 · 7,252 matching rows.
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Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.