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 138 of 153 · 3,057 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Joint and Muscle Pain MENTHOL Shaklee Corporation 3943824f-1f4f-4d6f-bd73-0b1be02162a5 2024-01-30 Warnings Exact identifier application number: M017 Mirakel Pain Relief Roll-On LIDOCAINE HCL Sanvio, Inc. 102f3618-13ad-37e3-e063-6294a90a8086 2024-01-30 Warnings Exact identifier application number: M017 Blistex Lip Medex PETROLATUM, MENTHOL, UNSPECIFIED FORM, CAMPHOR (SYNTHETIC), AND PHENOL Blistex Inc. 8ad39005-9419-4f1a-a1ae-2f76d212455e 2024-01-26 Warnings Exact identifier application number: M017 Point Relief Cold Spot Pain Relieving MENTHOL Fabrication Enterprises ad5d6f04-15e6-4548-95c2-32271c186bc1 2024-01-25 Warnings Exact identifier application number: M017 MIND BODY MATRIX PAIN RELIEF MENTHOL Functional Energetic, Inc. 3667dd0d-942e-4101-ba98-cb013ae77cf5 2024-01-25 Warnings Exact identifier application number: M017 SUPER WHITE STUFF Pain Relief MENTHOL BLUE SPRING WELLNESS e6d27df5-118c-4c6d-86e8-7b4401a39c76 2024-01-23 Warnings Exact identifier application number: M017 Burn First Aid BURN FIRST AID Dynarex Corporation 826e08be-dffa-5a27-e053-2a91aa0a8701 2024-01-22 Warnings Exact identifier application number: M017 Target Up and Up Pain Relief Menthol Topical Analgesic Roll-On MENTHOL TARGET CORPORATION 0f95fc55-8665-9e89-e063-6394a90a7891 2024-01-22 Warnings Exact identifier application number: M017 CVS Health Lidocaine Pain Relief Plus Menthol LIDOCAINE, MENTHOL, UNSPECIFIED FORM Natural Essentials, Inc. 77978069-a1b4-473e-83c9-8320e00eea89 2024-01-19 Warnings Exact identifier application number: M017 ZIMS MAX FREEZE LEG CRAMPS CAMPHOR, MENTHOL KOBAYASHI Healthcare International, Inc. ba26635d-95d3-4d88-93cc-1fd4fd29fd79 2024-01-18 Warnings Exact identifier application number: M017 Burn LIDOCAINE HART Health e95ebdac-9789-41c2-97da-2307e4538794 2024-01-18 Warnings Exact identifier application number: M017 Medi-First Hydrocortisone 1% HYDROCORTISONE ACETATE Unifirst First Aid Corporation bd216f5d-f304-7d8d-e053-2a95a90aa9ce 2024-01-17 Warnings Exact identifier application number: M017 Green Guard Hydrocortisone 1% HYDROCORTISONE Unifirst First Aid Corporation bd348e2a-57b1-3f17-e053-2a95a90a8bdc 2024-01-17 Warnings Exact identifier application number: M017 Pain Relief LIDOCAINE, MENTHOL HUMN Pharmaceuticals Inc 6c96f94a-e724-eab3-e053-2991aa0aab88 2024-01-17 Warnings Exact identifier application number: M017 CVS Health Lidocaine Pain Relief LIDOCAINE Natural Essentials, Inc. 52e82e70-53b7-4ecb-be39-fe10c94cc444 2024-01-17 Warnings Exact identifier application number: M017 CVS Health XL Lidocaine Pain Relief LIDOCAINE NATURAL ESSENTIALS, INC. ec16da91-8244-402b-b8d8-84896094ac2c 2024-01-17 Warnings Exact identifier application number: M017 Anti-itch DIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATE Target Corporation f444b0a6-2ed3-4236-8206-342150290675 2024-01-17 Warnings Exact identifier application number: M017 Maximum Strength Hydrocortisone Anti-itch HYDROCORTISONE 1% Target Corporation 4ff39cb8-3a20-4fe7-9829-1e882a484668 2024-01-17 Warnings Exact identifier application number: M017 Salonpas Pain Relieving LIDOCAINE 4% FLEX LIDOCAINE Hisamitsu Pharmaceutical Co., Inc. 9507f727-c49f-4de4-9d64-b6d977d568ab 2024-01-17 Warnings Exact identifier application number: M017 Burn LIDOCAINE HYDROCHLORIDE Nantong Health & Beyond Hygienic Products Inc. eca272cb-ac8f-982b-e053-2995a90aa8b2 2024-01-15 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