Wish ultra winter ice

Product NDC
84809-008
11-digit product format
848090008
Labeler code
84809
Product ID
84809-008_3b4d3df6-aa44-e03a-e063-6294a90a1b9c
Type
HUMAN OTC DRUG
Nonproprietary name
Menthol
Dosage form
GEL
Route
TOPICAL
Labeler
LJ Pharma
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-07-25
Substance
MENTHOL, UNSPECIFIED FORM
Active strength
2 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
Wish ultra winter ice
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MENTHOL, UNSPECIFIED FORM2 g/100g

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
311502Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
b4c5487c-1314-4d63-96df-077e72e7ee95Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84809-008-01Wish ultra winter ice200 g in 1 BOTTLEGEL2001

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 89 of 153 · 3,057 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Lidocaine PatchLIDOCAINEShenzhen Finona Information Technology Co., Ltd3875bde5-2e1a-5fdf-e063-6294a90a3c0d2025-06-26WarningsExact identifier
application number: M017
SupreH Bee Venom Arthritis Pain Relieving CreamSUPREH BEE VENOM ARTHRITIS PAIN RELIEVING CREAMShenzhen Xinxin Yunhai Technology Co., Ltd.3876cc44-7f3a-b084-e063-6294a90a61422025-06-26WarningsExact identifier
application number: M017
MediBalmHYDROCORTISONEBalmRx, LLC324dd151-84c5-3e2f-e063-6394a90a569d2025-06-26WarningsExact identifier
application number: M017
PHIZICO Pain ReliefMENTHOLER3 BRANDS INC.72715dc5-d1e7-4b4b-8e28-4e367abba3222025-06-25WarningsExact identifier
application number: M017
Diva Cramp Care CreamMETHYL SALICYLATE, MENTHOL, CAMPHORAvaria Health & Beauty Corp37368566-b14e-4d5c-bdde-6eea9073974f2025-06-25WarningsExact identifier
application number: M017
H2Ocean NOTHING TATTOO GLIDE AFTERCARE MAX STRENGTHLIDOCAINE HCLH2Ocean, LLC386bf11b-1d71-44bf-e063-6394a90a28172025-06-25WarningsExact identifier
application number: M017
Burn Relief Extra Strength Kool-DownLIDOCAINE - 3.9%Kool-Down Inc827fec2f-db3c-adbb-e053-2a91aa0a7c172025-06-25WarningsExact identifier
application number: M017
Hilook Blue Gel AnestheticLIDOCAINEGuangdong Aimu Biological Technology Co., Ltd1b9db681-a297-5aa9-e063-6394a90a80ea2025-06-25WarningsExact identifier
application number: M017
Hilook Numbing CreamLIDOCAINEGuangdong Aimu Biological Technology Co., Ltd1b9f1a4c-ca0b-d820-e063-6394a90a32392025-06-25WarningsExact identifier
application number: M017
Lidocaine Knee Pain Relief Gel-PatchLIDOCAINEGuangzhou Zhupuyou E-commerce Co., Ltd384c1ff8-80bd-86cb-e063-6394a90a2d652025-06-24WarningsExact identifier
application number: M017
Aroamas Cot Nicotine Transdermal Patches KitNICOTINE TRANSDERMAL PATCHESPCHEERY LLC38576022-9413-c9af-e063-6294a90afd462025-06-24WarningsExact identifier
application number: M017
NERVE REVERSE PAIN RELIEFMENTHOLPogue Medical Servicesda97bcc6-5aa8-48e2-a2c2-c937745bf6d32025-06-23WarningsExact identifier
application number: M017
Medterra Pain Relief Menthol Roll-OnMENTHOLRespect Manufacturing Corporation05a6067a-287a-52d4-e063-6394a90a2c4e2025-06-23WarningsExact identifier
application number: M017
Medterra Pain Relief 500mg Hemp Menthol CreamMENTHOLRespect Manufacturing Corporation06c4640a-ee42-5d1a-e063-6394a90ad2542025-06-23WarningsExact identifier
application number: M017
Medterra Pain Relief 1000mg Hemp Menthol CreamMENTHOLRespect Manufacturing Corporation06e944e8-71f6-9fe9-e063-6294a90a8c372025-06-23WarningsExact identifier
application number: M017
Procure gelMENTHOLTWIN MED, LLCe69c0b68-d408-9fd2-e053-2a95a90ac9342025-06-20WarningsExact identifier
application number: M017
A Health Itch Relief GelITCH RELIEF GELBionpharma, Inc.38040732-48c9-3533-e063-6394a90af10a2025-06-20WarningsExact identifier
application number: M017
SCHOELIF Numbing CreamNUMBING CREAMGuangzhou Qiexiran Cosmetics Co., Ltd.37eaabb7-884e-0bd5-e063-6294a90ae0632025-06-19WarningsExact identifier
application number: M017
Re-Lieved Lidocaine PatchLIDOCAINE PATCH 4%Transfer Technology37ee539c-df7e-511d-e063-6394a90a44692025-06-19WarningsExact identifier
application number: M017
Re-Lieved Lidocaine PatchLIDOCAINE PATCH 4%Transfer Technology37eef80a-556f-b090-e063-6294a90a151b2025-06-19WarningsExact identifier
application number: M017

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
311502menthol 2 % Topical GelPSNb4c5487c-1314-4d63-96df-077e72e7ee951
311502menthol 0.02 MG/MG Topical GelSCDb4c5487c-1314-4d63-96df-077e72e7ee951
311502menthol 2 % Topical GelSYb4c5487c-1314-4d63-96df-077e72e7ee951
311502menthol 2 % topical stickSYb4c5487c-1314-4d63-96df-077e72e7ee951

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
84809-008-0184809000801200 g in 1 BOTTLE (84809-008-01) 200 g2025-07-25NoNoCurrent