Home NDC 49873-705 TACT
Product NDC 49873-705
11-digit product format 498730705
Labeler code 49873
Product ID 49873-705_0bb93753-9288-eb0b-e063-6394a90a950b
Type HUMAN OTC DRUG
Nonproprietary name diphenhydramine hydrochloride, menthol
Dosage form CREAM
Route TOPICAL
Labeler Sato Pharmaceutical Inc., Ltd.
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 1997-09-09
Substance DIPHENHYDRAMINE HYDROCHLORIDE; LEVOMENTHOL
Active strength 2; 1 g/100g; g/100g
Pharmacologic classes Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
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 TACT
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DIPHENHYDRAMINE HYDROCHLORIDE 2 g/100g LEVOMENTHOL 1 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination TC2D6JAD40 Internal UNII lookup BZ1R15MTK7 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1245398 Internal RxNorm lookup 1245403 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 49873-705-01 TACT 20 g in 1 TUBE CREAM 20 4 49873-705-01 TACT 1 in 1 CARTON CREAM 1 4
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded DIPHENHYDRAMINE HYDROCHLORIDE ACTIVE INGREDIENT TC2D6JAD40 TACT (DIPHENHYDRAMINE HYDROCHLORIDE, MENTHOL) CREAM [SATO PHARMACEUTICAL INC., LTD.] 1 LEVOMENTHOL ACTIVE INGREDIENT BZ1R15MTK7 TACT (DIPHENHYDRAMINE HYDROCHLORIDE, MENTHOL) CREAM [SATO PHARMACEUTICAL INC., LTD.] 1 DIPHENHYDRAMINE ACTIVE MOIETY 8GTS82S83M TACT (DIPHENHYDRAMINE HYDROCHLORIDE, MENTHOL) CREAM [SATO PHARMACEUTICAL INC., LTD.] 1 MENTHOL ACTIVE MOIETY L7T10EIP3A TACT (DIPHENHYDRAMINE HYDROCHLORIDE, MENTHOL) CREAM [SATO PHARMACEUTICAL INC., LTD.] 1 BUTYLPARABEN INACTIVE INGREDIENT 3QPI1U3FV8 TACT (DIPHENHYDRAMINE HYDROCHLORIDE, MENTHOL) CREAM [SATO PHARMACEUTICAL INC., LTD.] 1 CARBOMER HOMOPOLYMER TYPE C INACTIVE INGREDIENT 4Q93RCW27E TACT (DIPHENHYDRAMINE HYDROCHLORIDE, MENTHOL) CREAM [SATO PHARMACEUTICAL INC., LTD.] 1 CETYL ALCOHOL INACTIVE INGREDIENT 936JST6JCN TACT (DIPHENHYDRAMINE HYDROCHLORIDE, MENTHOL) CREAM [SATO PHARMACEUTICAL INC., LTD.] 1 DIETHANOLAMINE INACTIVE INGREDIENT AZE05TDV2V TACT (DIPHENHYDRAMINE HYDROCHLORIDE, MENTHOL) CREAM [SATO PHARMACEUTICAL INC., LTD.] 1 EDETATE SODIUM INACTIVE INGREDIENT MP1J8420LU TACT (DIPHENHYDRAMINE HYDROCHLORIDE, MENTHOL) CREAM [SATO PHARMACEUTICAL INC., LTD.] 1 LIGHT MINERAL OIL INACTIVE INGREDIENT N6K5787QVP TACT (DIPHENHYDRAMINE HYDROCHLORIDE, MENTHOL) CREAM [SATO PHARMACEUTICAL INC., LTD.] 1 PEG-40 STEARATE INACTIVE INGREDIENT ECU18C66Q7 TACT (DIPHENHYDRAMINE HYDROCHLORIDE, MENTHOL) CREAM [SATO PHARMACEUTICAL INC., LTD.] 1 PETROLATUM INACTIVE INGREDIENT 4T6H12BN9U TACT (DIPHENHYDRAMINE HYDROCHLORIDE, MENTHOL) CREAM [SATO PHARMACEUTICAL INC., LTD.] 1 PROPYLENE GLYCOL INACTIVE INGREDIENT 6DC9Q167V3 TACT (DIPHENHYDRAMINE HYDROCHLORIDE, MENTHOL) CREAM [SATO PHARMACEUTICAL INC., LTD.] 1 PROPYLPARABEN INACTIVE INGREDIENT Z8IX2SC1OH TACT (DIPHENHYDRAMINE HYDROCHLORIDE, MENTHOL) CREAM [SATO PHARMACEUTICAL INC., LTD.] 1 SORBITAN MONOSTEARATE INACTIVE INGREDIENT NVZ4I0H58X TACT (DIPHENHYDRAMINE HYDROCHLORIDE, MENTHOL) CREAM [SATO PHARMACEUTICAL INC., LTD.] 1 WATER INACTIVE INGREDIENT 059QF0KO0R TACT (DIPHENHYDRAMINE HYDROCHLORIDE, MENTHOL) CREAM [SATO PHARMACEUTICAL INC., LTD.] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 49873-705 TACT (DIPHENHYDRAMINE HYDROCHLORIDE, MENTHOL) CREAM [SATO PHARMACEUTICAL INC., LTD.] 4 Current NDC, Legacy NDC, 2 package rows 20231205_b6e2ee24-69de-4dfd-9081-b9537b7a7bad.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 115 of 153 · 3,057 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Serum X LIDOCAINE HYDROCHLORIDE AO Biologix, LLC e07b6268-6400-6849-e053-2a95a90a8b3e 2024-12-11 Warnings Exact identifier application number: M017 PlusCBD Pain Cream (Penetrating) 2oz CAMPHOR, MENTHOL CV Sciences, Inc. ca39d327-6bf3-3408-e053-2a95a90af2d5 2024-12-11 Warnings Exact identifier application number: M017 Blistex Medicated DIMETHICONE, CAMPHOR (SYNTHETIC), MENTHOL, AND PHENOL Blistex Inc. e95439d3-f12b-4c1c-999a-79f2ddba4cfb 2024-12-11 Warnings Exact identifier application number: M017 Blistex Foille Medicated First Aid BENZOCAINE AND CHLOROXYLENOL Blistex Inc. e2eca808-e97b-43e0-aa51-7025cc61c7a8 2024-12-11 Warnings Exact identifier application number: M017 Hydrocortisone HYDROCORTISONE J&A Digital Inc. ff95a536-35b3-4006-b43c-cce359e86aa9 2024-12-10 Warnings Exact identifier application number: M017 TheraCare Maximum Strength Pain Relief Patch LIDOCAINE Veridian Healthcare dfaf8a77-2276-4791-e053-2a95a90a3288 2024-12-10 Warnings Exact identifier application number: M017 Methyl Salicylate METHYL SALICYLATE Alexso, Inc eef555d3-f23d-4847-93f3-fa7a06072a0f 2024-12-09 Warnings Exact identifier application number: M017 Lidocaine 4 Percent LIDOCAINE SA3, LLC 651710db-3c50-4bcf-b7cc-9ed24f663427 2024-12-09 Warnings Exact identifier application number: M017 HealthWise Pain Relief Lidocaine Patch LIDOCAINE 4% Veridian Healthcare 28db1c03-d01f-83ea-e063-6294a90aee26 2024-12-09 Warnings Exact identifier application number: M017 Joint and Muscle Pain Relief MENTHOL Allure Labs e82f99fd-c2ef-686f-e053-2a95a90a1dc9 2024-12-09 Warnings Exact identifier application number: M017 Tough Love Pain Relieving LIDOCAINE HCL Allure Labs ee8c1a2b-36ef-6fd7-e053-2a95a90a9c01 2024-12-09 Warnings Exact identifier application number: M017 Capsaicin CAPSAICIN SA3, LLC 5617e91d-e650-4a0d-8565-b8288ea41c77 2024-12-09 Warnings Exact identifier application number: M017 Medicaine Sting and Bite BENZOCAINE James Alexander Corporation 753e6cbe-31e0-4017-93d0-8b4bf5972f37 2024-12-09 Warnings Exact identifier application number: M017 AUVON Pain Relief Roll-on MENTHOL SHENZHEN YUWEN E-COMMERCE CO., LTD. df239c4d-af6a-41ca-baed-d0788782ce9f 2024-12-08 Warnings Exact identifier application number: M017 AUVON Pain Relief Roll-on LIDOCAINE SHENZHEN YUWEN E-COMMERCE CO., LTD. 8b30f623-6077-4f2e-8fa4-ce4a298953b5 2024-12-08 Warnings Exact identifier application number: M017 QC Medicated anti itch PRAMOXINE HYDROCHLORIDE, MENTHOL Chain Drug Marketing Association b5e41e3a-81df-3a63-e053-2a95a90a5839 2024-12-08 Warnings Exact identifier application number: M017 QC Lidocaine Maximum Strength LIDOCAINE HCL Chain Drug Marketing Association b5e1b1ab-8a95-2d2d-e053-2995a90aea53 2024-12-08 Warnings Exact identifier application number: M017 Capsaicin CAPSAICIN Alexso, Inc 433da27d-04fb-481a-bbb0-874bb72c806a 2024-12-06 Warnings Exact identifier application number: M017 POMG PAIN RELIEF BODY LIDOCAINE POMG LLC 28d7ac46-b27f-43bb-e063-6294a90a93ed 2024-12-06 Warnings Exact identifier application number: M017 Capsaicin 0.1 Percent CAPSAICIN Alexso, Inc 0090ca38-6433-45c4-9453-edf2788c14c6 2024-12-06 Warnings Exact identifier application number: M017
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 49873-705-01 49873070501 1 TUBE in 1 CARTON (49873-705-01) / 20 g in 1 TUBE 1 tube 1997-09-09 0000-00-00 No No Current