Home NDC 61477-101 ALOE ICE SUNBURN RELIEF
Product NDC 61477-101
11-digit product format 614770101
Labeler code 61477
Product ID 61477-101_497adb6b-44dd-ceee-e063-6294a90a52cc
Type HUMAN OTC DRUG
Nonproprietary name LIDOCAINE HYDROCHLORIDE
Dosage form GEL
Route TOPICAL
Labeler Aloe Care International, LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2014-02-24
Substance LIDOCAINE HYDROCHLORIDE
Active strength 2 g/100mL
Pharmacologic classes Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 6 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2022-04-09 23:13 UTC · source 2022-04-08 excluded product product 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 61477-101-11 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 61477-101-14 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 excluded product product bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 61477-101-11 bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 61477-101-14 bd6a592717d7…303034d00443…
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 ALOE ICE SUNBURN RELIEF
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LIDOCAINE HYDROCHLORIDE 2 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination V13007Z41A Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1011852 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 61477-101-11 ALOE ICE SUNBURN RELIEF 60 mL in 1 TUBE GEL 60 11 61477-101-14 ALOE ICE SUNBURN RELIEF 120 mL in 1 TUBE GEL 120 11
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded LIDOCAINE HYDROCHLORIDE ACTIVE INGREDIENT V13007Z41A ALOE ICE SUNBURN RELIEF JELLY (LIDOCAINE HYDROCHLORIDE) GEL [ALOE CARE INTERNATIONAL, LLC] 3 LIDOCAINE ACTIVE MOIETY 98PI200987 ALOE ICE SUNBURN RELIEF JELLY (LIDOCAINE HYDROCHLORIDE) GEL [ALOE CARE INTERNATIONAL, LLC] 3 ALOE VERA WHOLE INACTIVE INGREDIENT KIZ4X2EHYX ALOE ICE SUNBURN RELIEF JELLY (LIDOCAINE HYDROCHLORIDE) GEL [ALOE CARE INTERNATIONAL, LLC] 3 CARBOMER 934 INACTIVE INGREDIENT Z135WT9208 ALOE ICE SUNBURN RELIEF JELLY (LIDOCAINE HYDROCHLORIDE) GEL [ALOE CARE INTERNATIONAL, LLC] 3 EDETATE DISODIUM INACTIVE INGREDIENT 7FLD91C86K ALOE ICE SUNBURN RELIEF JELLY (LIDOCAINE HYDROCHLORIDE) GEL [ALOE CARE INTERNATIONAL, LLC] 3 FD&C BLUE NO. 1 INACTIVE INGREDIENT H3R47K3TBD ALOE ICE SUNBURN RELIEF JELLY (LIDOCAINE HYDROCHLORIDE) GEL [ALOE CARE INTERNATIONAL, LLC] 3 IODOPROPYNYL BUTYLCARBAMATE INACTIVE INGREDIENT 603P14DHEB ALOE ICE SUNBURN RELIEF JELLY (LIDOCAINE HYDROCHLORIDE) GEL [ALOE CARE INTERNATIONAL, LLC] 3 METHYLISOTHIAZOLINONE INACTIVE INGREDIENT 229D0E1QFA ALOE ICE SUNBURN RELIEF JELLY (LIDOCAINE HYDROCHLORIDE) GEL [ALOE CARE INTERNATIONAL, LLC] 3 POLYSORBATE 20 INACTIVE INGREDIENT 7T1F30V5YH ALOE ICE SUNBURN RELIEF JELLY (LIDOCAINE HYDROCHLORIDE) GEL [ALOE CARE INTERNATIONAL, LLC] 3 PROPYLENE GLYCOL INACTIVE INGREDIENT 6DC9Q167V3 ALOE ICE SUNBURN RELIEF JELLY (LIDOCAINE HYDROCHLORIDE) GEL [ALOE CARE INTERNATIONAL, LLC] 3 TROLAMINE INACTIVE INGREDIENT 9O3K93S3TK ALOE ICE SUNBURN RELIEF JELLY (LIDOCAINE HYDROCHLORIDE) GEL [ALOE CARE INTERNATIONAL, LLC] 3 WATER INACTIVE INGREDIENT 059QF0KO0R ALOE ICE SUNBURN RELIEF JELLY (LIDOCAINE HYDROCHLORIDE) GEL [ALOE CARE INTERNATIONAL, LLC] 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 61477-101 ALOE ICE SUNBURN RELIEF (LIDOCAINE HYDROCHLORIDE) GEL [ALOE CARE INTERNATIONAL, LLC] 10 Current NDC, Legacy NDC, 2 package rows 20240214_56866fa8-052e-497c-a954-978d7d628949.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 23 of 153 · 3,057 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Kevo-Prophen JUNIPER TAR Faeve, LLC 4fe773a8-77cd-831e-e063-6294a90ae2ca 2026-04-20 Warnings Exact identifier application number: M017 BeeVenom METHYL SALICYLATE Menper Distributors, Inc. 4fe7a986-336d-ad4e-e063-6294a90a0b8a 2026-04-20 Warnings Exact identifier application number: M017 Benzodent BENZOCAINE Focus Consumer Healthcare, LLC 5fdcb871-d387-6352-e053-2991aa0a09da 2026-04-20 Warnings Exact identifier application number: M017 Tecnu Calagel DIPHENHYDRAMINE HYDROCHLORIDE Tec Laboratories Inc. 8bc9cbfe-1dd4-18ed-e053-2a95a90a7966 2026-04-20 Warnings Exact identifier application number: M017 Aemerry Numbing Cream MENTHOL 5% Da Capo Prima LLC 4fefddaf-19c8-86b4-e063-6294a90abffc 2026-04-20 Warnings Exact identifier application number: M017 Sting Relief Swab BENZOCAINE 4 Visions LLC 4fc7a356-2f1d-85af-e063-6394a90aec6b 2026-04-18 Warnings Exact identifier application number: M017 Equate Lidocaine and Menthol Paraben Free LIDOCAINE 4% PLUS MENTHOL 1% Walmart Stores Inc 4fa917de-bc46-0b8d-e063-6294a90a218a 2026-04-17 Warnings Exact identifier application number: M017 LidoPro LIDOCAINE AND MENTHOL Advanced Rx of Tennessee, LLC 4faa515f-6040-d948-e063-6294a90a187f 2026-04-17 Warnings Exact identifier application number: M017 Coleman Bite and Sting Relief EXTERNAL ANESTHETIC AND FIRST AID ANTISEPTIC Wisconsin Pharmacal Company 4fadf1f1-478a-5104-e063-6294a90a10cb 2026-04-17 Warnings Exact identifier application number: M017 Ice Gel ICE COLD ANALGESIC MENTHOL Universal Distribution Center LLC 4f921ced-7722-cba5-e063-6294a90a650b 2026-04-16 Warnings Exact identifier application number: M017 Walgreens Capsaicin Hot Patch CAPSAICIN Walgreen Co. 41e959d8-f6ac-f5b4-e063-6294a90abd96 2026-04-16 Warnings Exact identifier application number: M017 Walgreens Cold Therapy Pain Relieving Patch MENTHOL Walgreen Co. 41e7574a-348f-8eb8-e063-6294a90a6e90 2026-04-16 Warnings Exact identifier application number: M017 Coleman Sting and Bite Relief EXTERNAL ANALGESIC AND FIRST AID ANTISEPTIC Wisconsin Pharmacal Company 4f94ab35-3099-716c-e063-6294a90a8bea 2026-04-16 Warnings Exact identifier application number: M017 Kroger Witch Hazel WITCH HAZEL Kroger Co. 461407d0-fbf6-47e9-e063-6394a90a9a83 2026-04-16 Warnings Exact identifier application number: M017 Stopain Extra Strength Gel MENTHOL Troy Manufacturing, Inc. 86fe4e8c-5279-445a-a19a-e694eac785fd 2026-04-16 Warnings Exact identifier application number: M017 Stopain Clinical MENTHOL, UNSPECIFIED FORM Troy Manufacturing, Inc. 4503208f-2808-4727-8066-c431230bd70b 2026-04-16 Warnings Exact identifier application number: M017 EXTRA STRENGTH STOPAIN COLD PAIN RELIEVING ROLL ON MENTHOL TROY MANUFACTURING, INC 895896dc-0762-40a7-8313-cca10ce68984 2026-04-16 Warnings Exact identifier application number: M017 HealthWise Medicated Cold Hot 5% MENTHOL Veridian Healthcare 4f9b1b2d-1acc-e0a7-e063-6394a90aadbc 2026-04-16 Warnings Exact identifier application number: M017 Lidoease 2% LIDOCAINE HCL 2% PureTek Corporation 3ba0c0ff-0f7a-7a29-e063-6294a90a547a 2026-04-16 Warnings Exact identifier application number: M017 Walgreens Lidocaine Pain Relieving Patch Assorted LIDOCAINE Walgreen Co. 41e98f15-669f-4543-e063-6294a90a1ef7 2026-04-15 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 61477-101-11 61477010111 60 mL in 1 TUBE (61477-101-11) 60 ml 2014-02-24 0000-00-00 No No Current 61477-101-14 61477010114 120 mL in 1 TUBE (61477-101-14) 120 ml 2014-02-24 0000-00-00 No No Current