PLANTAR FASCIITIS Relief Gel Roll-On

Product NDC
84165-012
11-digit product format
841650012
Labeler code
84165
Product ID
84165-012_37570149-dae2-a4f2-e063-6294a90a3245
Type
HUMAN OTC DRUG
Nonproprietary name
Menthol
Dosage form
GEL
Route
TOPICAL
Labeler
Guangzhou Zhupuyou E-commerce Co., Ltd
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-06-12
Substance
MENTHOL
Active strength
4 g/100mL
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
PLANTAR FASCIITIS Relief Gel Roll-On
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MENTHOL4 g/100mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

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

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
415974Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
37570149-dae1-a4f2-e063-6294a90a3245Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84165-012-01PLANTAR FASCIITIS Relief Gel Roll-On74 mL in 1 BOTTLEGEL741
84165-012-01PLANTAR FASCIITIS Relief Gel Roll-On1 in 1 BOXGEL11
84165-012-02PLANTAR FASCIITIS Relief Gel Roll-On2 in 1 BOXGEL21
84165-012-02PLANTAR FASCIITIS Relief Gel Roll-On74 mL in 1 BOTTLEGEL741
84165-012-03PLANTAR FASCIITIS Relief Gel Roll-On74 mL in 1 BOTTLEGEL741
84165-012-03PLANTAR FASCIITIS Relief Gel Roll-On3 in 1 BOXGEL31
84165-012-04PLANTAR FASCIITIS Relief Gel Roll-On74 mL in 1 BOTTLEGEL741
84165-012-04PLANTAR FASCIITIS Relief Gel Roll-On4 in 1 BOXGEL41
84165-012-05PLANTAR FASCIITIS Relief Gel Roll-On74 mL in 1 BOTTLEGEL741
84165-012-05PLANTAR FASCIITIS Relief Gel Roll-On5 in 1 BOXGEL51
84165-012-06PLANTAR FASCIITIS Relief Gel Roll-On6 in 1 BOXGEL61
84165-012-06PLANTAR FASCIITIS Relief Gel Roll-On74 mL in 1 BOTTLEGEL741
84165-012-07PLANTAR FASCIITIS Relief Gel Roll-On74 mL in 1 BOTTLEGEL741
84165-012-07PLANTAR FASCIITIS Relief Gel Roll-On7 in 1 BOXGEL71
84165-012-08PLANTAR FASCIITIS Relief Gel Roll-On74 mL in 1 BOTTLEGEL741
84165-012-08PLANTAR FASCIITIS Relief Gel Roll-On8 in 1 BOXGEL81
84165-012-09PLANTAR FASCIITIS Relief Gel Roll-On9 in 1 BOXGEL91
84165-012-09PLANTAR FASCIITIS Relief Gel Roll-On74 mL in 1 BOTTLEGEL741
84165-012-10PLANTAR FASCIITIS Relief Gel Roll-On74 mL in 1 BOTTLEGEL741
84165-012-10PLANTAR FASCIITIS Relief Gel Roll-On10 in 1 BOXGEL101

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 139 of 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Dendracin NeurodendraxcinMETHYL SALICYLATE, MENTHOL AND CAPSAICINProficient Rx LP7e765fc1-74c6-4af3-a9cf-05b57011d7d82024-01-01WarningsExact identifier
application number: M017
CeraVe Developed with Dermatologists Itch Relief MoisturizingPRAMOXINE HYDROCHLORIDEL'Oreal USA Products Incc6a0880e-fc16-46e9-8314-c56c9d15bf312023-12-31WarningsExact identifier
application number: M017
CeraVe Developed with Dermatologists Anti ItchHYDROCORTISONEL'Oreal USA Products Inc.8d65e945-2557-486f-9279-ecbaa08f31c42023-12-31WarningsExact identifier
application number: M017
Nighttime Sleep-Aid Non-Habit FormingDIPHENHYDRAMINE HCIAptaPharma Inc.ed0ba7aa-e794-43da-b576-6b9945bf74772023-12-30WarningsExact identifier
application number: M017
Sting-KillBENZOCAINE AND MENTHOLRANDOB LABS, LTD. DBA CROSSINGWELL CONSUMER HEALTHb8bd9280-f20a-4b2a-aef7-a0ba7b3b87012023-12-29WarningsExact identifier
application number: M017
Maybelline New York Baby Lips Dr Rescue Medicated BalmMENTHOLL'Oreal USA Products Inc2f7b8221-66f6-4aed-8359-318cfc656a722023-12-28WarningsExact identifier
application number: M017
Equate CortisoneHYDROCORTISONE 1%Walmart Inc027fae33-93a0-a61f-e063-6294a90a990f2023-12-27WarningsExact identifier
application number: M017
Walgreens Cool n Heat LidocaineLIDOCAINE HCL 4%Walgreens Co0681c6c5-5a8b-ea9e-e063-6394a90a83bc2023-12-27WarningsExact identifier
application number: M017
EXTRA STRENGTH WAL-DRYL ITCH RELIEFDIPHENHYDRAMINE, ZINC ACETATEWALGREEN CO681cf1af-2cc3-4e6d-b76f-f00731ea3e122023-12-27WarningsExact identifier
application number: M017
XRay Pain ReliefMENTHOL, (PLUS)-, CAMPHOR, (-)-, AND METHYL SALICYLATEGenomma Lab USA5244ddee-fd9e-4df3-8fb3-b16aa321a3162023-12-27WarningsExact identifier
application number: M017
Camphor SpiritCAMPHOR 10%Pharma Nobis, LLCe42fbe63-b01c-4f85-e053-2a95a90a51432023-12-26WarningsExact identifier
application number: M017
Equate CalasprayPRAMOXINE HCL 1%, ZINC ACETATE 0.1%Walmart Inc027ed5ab-05ec-569f-e063-6394a90abbc32023-12-26WarningsExact identifier
application number: M017
EXTERNAL ANALGESICCAMPHOR, CAPSICUM, MENTHOLHmong 213b6155a5-51aa-2780-e054-00144ff8d46c2023-12-26WarningsExact identifier
application number: M017
LEADER Camphor SpiritCAMPHOR (NATURAL)Cardinal Health, 110 dba Leader7d3b0b28-5190-0622-e053-2991aa0af5612023-12-22WarningsExact identifier
application number: M017
Antiseptic Instant Pain ReliefCAMPHOR 10.8% AND PHENOL 4.7%Pharma Nobis, LLCe42f484d-a642-3489-e053-2a95a90a42542023-12-22WarningsExact identifier
application number: M017
Itch Relief GelITCH RELIEF GELPharma Nobis, LLCe42f484d-a641-3489-e053-2a95a90a42542023-12-22WarningsExact identifier
application number: M017
Witch HazelWITCH HAZELPharma Nobis, LLCe42f484d-a644-3489-e053-2a95a90a42542023-12-22WarningsExact identifier
application number: M017
Dermoplast Pain relievingBENZOCAINE, MENTHOLAdvantice Healthdad00c95-4e11-3eec-e053-2a95a90a7a182023-12-21WarningsExact identifier
application number: M017
equate Maximum Strength Pain Relieving 4% Lidocaine with Lavender Essential Oil Topical analgesicLIDOCAINE HYDROCHLORIDEWal-Mart Stores, Inc.bf954949-a7b7-44ba-8565-f1d5c0a6c0d12023-12-21WarningsExact identifier
application number: M017
Bactine Max BandageLIDOCAINEWellSpring Pharmaceutical Corporation465dc46e-6435-4569-9516-f648d0fe0f092023-12-21WarningsExact identifier
application number: M017

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
415974menthol 4 % Topical GelPSN37570149-dae1-a4f2-e063-6294a90a32451
415974menthol 0.04 MG/MG Topical GelSCD37570149-dae1-a4f2-e063-6294a90a32451
415974menthol 4 % Topical GelSY37570149-dae1-a4f2-e063-6294a90a32451

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
84165-012-01841650012011 BOTTLE in 1 BOX (84165-012-01) / 74 mL in 1 BOTTLE1 bottle2025-06-12NoNoCurrent
84165-012-02841650012022 BOTTLE in 1 BOX (84165-012-02) / 74 mL in 1 BOTTLE2 bottle2025-06-12NoNoCurrent
84165-012-03841650012033 BOTTLE in 1 BOX (84165-012-03) / 74 mL in 1 BOTTLE3 bottle2025-06-12NoNoCurrent
84165-012-04841650012044 BOTTLE in 1 BOX (84165-012-04) / 74 mL in 1 BOTTLE4 bottle2025-06-12NoNoCurrent
84165-012-05841650012055 BOTTLE in 1 BOX (84165-012-05) / 74 mL in 1 BOTTLE5 bottle2025-06-12NoNoCurrent
84165-012-06841650012066 BOTTLE in 1 BOX (84165-012-06) / 74 mL in 1 BOTTLE6 bottle2025-06-12NoNoCurrent
84165-012-07841650012077 BOTTLE in 1 BOX (84165-012-07) / 74 mL in 1 BOTTLE7 bottle2025-06-12NoNoCurrent
84165-012-08841650012088 BOTTLE in 1 BOX (84165-012-08) / 74 mL in 1 BOTTLE8 bottle2025-06-12NoNoCurrent
84165-012-09841650012099 BOTTLE in 1 BOX (84165-012-09) / 74 mL in 1 BOTTLE9 bottle2025-06-12NoNoCurrent
84165-012-108416500121010 BOTTLE in 1 BOX (84165-012-10) / 74 mL in 1 BOTTLE10 bottle2025-06-12NoNoCurrent