FDA.reportPublic FDA data

EXTRA STRENGTH HUA TUO PAIN RELIEVING

Product NDC
69070-307
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
IngredientStrength
CAMPHOR (SYNTHETIC)3.1 g/100g
MENTHOL2.6 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
5TJD82A1ETInternal UNII lookup
L7T10EIP3AInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
2118540Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
9850754b-ac94-4ec6-b75a-8096e5ac9456Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69070-307-01EXTRA STRENGTH HUA TUO PAIN RELIEVING5 in 1 POUCHPLASTER55
69070-307-01EXTRA STRENGTH HUA TUO PAIN RELIEVING1 in 1 BOXPLASTER15

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69070-307EXTRA STRENGTH HUA TUO PAIN RELIEVING (CAMPHOR AND MENTHOL) PLASTER [ZHEJIANG DINGTAI PHARMACEUTICAL CO., LTD]4Current NDC, Legacy NDC, 2 package rows20241127_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 152 of 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Bactine Max Lidocaine Roll-on 2.5ozLIDOCAINEWellSpring Pharmaceutical Corporation09b32a98-9131-451e-87a6-81a1e4ed7ec52023-04-25WarningsExact identifier
application number: M017
Icy Hot Pro DryCAMPHOR, MENTHOLChattem, Inc.4de1bc29-d166-4599-9e75-5f841bf209672023-03-01WarningsExact identifier
application number: M017
Icy Hot Vanishing ScentMENTHOLChattem, Inc.e2092016-9741-433d-92e6-74bfddadb72c2022-09-29WarningsExact identifier
application number: M017
New TerocinMETHYL SALICYLATE, CAPSAICIN, AND MENTHOLAlexso, Inc5dbd5fc0-a27e-4979-aca7-28f73096fd5f2022-08-18WarningsExact identifier
application number: M017
FIRSTAR Sting Relief PadBENZOCAINEJIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD.0e491a7a-4204-439f-862d-741cbc0be9fd2021-07-06WarningsExact identifier
application number: M017
Arthritis Relief GoodSenseTROLAMINE SALICYLATEGeiss, Destin & Dunn, Inca253730a-2187-07de-e053-2a95a90a98772020-04-02WarningsExact identifier
application number: M017
Aloe CortHYDROCORTISONETopiderm, Inc.789a6669-3320-4558-8d6f-ab255db50d8d2019-09-17WarningsExact identifier
application number: M017
Eagle Brand Medicated Roll On RefreshCAMPHOR, MENTHOLBorden Company (Private) Limited567b6820-fb52-630e-e063-6294a90a8bf82015-07-01WarningsExact identifier
application number: M017
Eagle Brand Medicated Oil AromaticCAMPHOR, MENTHOL, METHYL SALICYLATEBorden Company (Private) Limited54e45d89-e8c3-6fc3-e063-6394a90aac4e2015-06-15WarningsExact identifier
application number: M017

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
2118540camphor 3.1 % / menthol 2.6 % Medicated PatchPSN9850754b-ac94-4ec6-b75a-8096e5ac94565
2118540camphor 0.031 MG/MG / menthol 0.026 MG/MG Medicated PatchSCD9850754b-ac94-4ec6-b75a-8096e5ac94565
2118540camphor 3.1 % / menthol 2.6 % Medicated PatchSY9850754b-ac94-4ec6-b75a-8096e5ac94565

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69070-307-01690700307011 POUCH in 1 BOX (69070-307-01) / 5 PATCH in 1 POUCH / 1 g in 1 PATCH1 pouch2019-04-090000-00-00NoNoCurrent