Home DailyMed 1faa2e19-0097-ea6a-e063-6394a90a41f5 POMG PAIN RELIEF BODY CREAM Drug label information. FDA.report displays public Structured Product Labeling data from DailyMed and legacy FDA.report DailyMed cache rows. This page is not medical advice, prescribing advice, or a substitute for the official label reviewed by a qualified healthcare professional. Labeling can change; when a current hydrated DailyMed SPL record is available, FDA.report shows that newer record before legacy cached files.
Manufacturer POMG LLC
Effective date 2024-09-27
Label type HUMAN OTC DRUG LABEL
Version 2
Source legacy-cache
Hydrated at 2026-08-01 20:53:53 Label at a glance# Product POMG PAIN RELIEF BODY
Active ingredient LIDOCAINE
Label structure 7 sections
Dosage and administration Directions • Adults and children 12 years of age and older: rub a thin film over desired area not more than 3 to 4 times daily • Children under 12 years of age: consult a doctor • If using on hands, avoid contact with eyes and mouth
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 84615-005 POMG PAIN RELIEF BODY (LIDOCAINE) CREAM [POMG LLC] 2 Unmatched 20240929_1faa2e19-0097-ea6a-e063-6394a90a41f5.zip
Products# Every source-derived product name is available through these pages.
DailyMed product names page 1 of 1 · 15 matching rows.
POMG PAIN RELIEF BODY Lidocaine JOJOBA OIL GRAPE SEED OIL ALMOND OIL SHEA BUTTER ARGAN OIL CANNABIS SATIVA SEED OIL ACEPROMAZINE ARNICA MONTANA COCOA BUTTER ROSA CANINA FRUIT OIL YELLOW WAX AVOCADO OIL MANGIFERA INDICA SEED BUTTER Ingredients# Every source-derived ingredient row is available through these pages.
DailyMed ingredient rows page 1 of 1 · 14 matching rows.
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 1 of 1 · 1 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.