Home NDC 69070-307-01 EXTRA STRENGTH HUA TUO PAIN RELIEVING
Product NDC 69070-307
Requested package NDC 69070-307-01
11-digit product format 690700307
Labeler code 69070
Product ID 69070-307_4345be21-4ba4-122d-e063-6394a90a5fa7
Type HUMAN OTC DRUG
Nonproprietary name Camphor and Menthol
Dosage form PLASTER
Route TRANSDERMAL
Labeler Zhejiang Dingtai Pharmaceutical Co., Ltd
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-04-09
Substance CAMPHOR (SYNTHETIC); MENTHOL
Active strength 3.1; 2.6 g/100g; g/100g
NDC exclude flag No
Listing certified through 2026-12-31
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 EXTRA STRENGTH HUA TUO PAIN RELIEVING
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CAMPHOR (SYNTHETIC) 3.1 g/100g MENTHOL 2.6 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 5TJD82A1ET Internal UNII lookup L7T10EIP3A Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2118540 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69070-307-01 EXTRA STRENGTH HUA TUO PAIN RELIEVING 5 in 1 POUCH PLASTER 5 5 69070-307-01 EXTRA STRENGTH HUA TUO PAIN RELIEVING 1 in 1 BOX PLASTER 1 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69070-307 EXTRA STRENGTH HUA TUO PAIN RELIEVING (CAMPHOR AND MENTHOL) PLASTER [ZHEJIANG DINGTAI PHARMACEUTICAL CO., LTD] 4 Current NDC, Legacy NDC, 2 package rows 20241127_9850754b-ac94-4ec6-b75a-8096e5ac9456.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 97 of 151 · 3,010 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 69070-307-01 69070030701 1 POUCH in 1 BOX (69070-307-01) / 5 PATCH in 1 POUCH / 1 g in 1 PATCH 1 pouch 2019-04-09 0000-00-00 No No Current