Home NDC 62217-200 Fruit of the Earth Aloe Vera Cool Blue
Product NDC 62217-200
11-digit product format 622170200
Labeler code 62217
Product ID 62217-200_1d9eb3d8-4244-1150-e063-6294a90a8ae0
Type HUMAN OTC DRUG
Nonproprietary name Lidocaine Hydrochloride
Dosage form GEL
Route TOPICAL
Labeler Fruit of the Earth, Inc.
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2014-09-10
Substance LIDOCAINE
Active strength 10 mg/g
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 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 Fruit of the Earth Aloe Vera Cool Blue
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LIDOCAINE 10 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 98PI200987 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1012204 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 62217-200-20 Fruit of the Earth Aloe Vera Cool Blue 567 g in 1 BOTTLE GEL 567 4
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded LIDOCAINE ACTIVE INGREDIENT 98PI200987 FRUIT OF THE EARTH ALOE VERA COOL BLUE (LIDOCAINE HYDROCHLORIDE) GEL [FRUIT OF THE EARTH, INC.] 2 LIDOCAINE ACTIVE MOIETY 98PI200987 FRUIT OF THE EARTH ALOE VERA COOL BLUE (LIDOCAINE HYDROCHLORIDE) GEL [FRUIT OF THE EARTH, INC.] 2 ALOE VERA LEAF INACTIVE INGREDIENT ZY81Z83H0X FRUIT OF THE EARTH ALOE VERA COOL BLUE (LIDOCAINE HYDROCHLORIDE) GEL [FRUIT OF THE EARTH, INC.] 2 CARBOMER 940 INACTIVE INGREDIENT 4Q93RCW27E FRUIT OF THE EARTH ALOE VERA COOL BLUE (LIDOCAINE HYDROCHLORIDE) GEL [FRUIT OF THE EARTH, INC.] 2 EDETATE SODIUM INACTIVE INGREDIENT MP1J8420LU FRUIT OF THE EARTH ALOE VERA COOL BLUE (LIDOCAINE HYDROCHLORIDE) GEL [FRUIT OF THE EARTH, INC.] 2 FD&C BLUE NO. 1 INACTIVE INGREDIENT H3R47K3TBD FRUIT OF THE EARTH ALOE VERA COOL BLUE (LIDOCAINE HYDROCHLORIDE) GEL [FRUIT OF THE EARTH, INC.] 2 ISOCETETH-20 INACTIVE INGREDIENT O020065R7Z FRUIT OF THE EARTH ALOE VERA COOL BLUE (LIDOCAINE HYDROCHLORIDE) GEL [FRUIT OF THE EARTH, INC.] 2 MAGNESIUM NITRATE INACTIVE INGREDIENT 77CBG3UN78 FRUIT OF THE EARTH ALOE VERA COOL BLUE (LIDOCAINE HYDROCHLORIDE) GEL [FRUIT OF THE EARTH, INC.] 2 MAGNESIUM SULFATE INACTIVE INGREDIENT DE08037SAB FRUIT OF THE EARTH ALOE VERA COOL BLUE (LIDOCAINE HYDROCHLORIDE) GEL [FRUIT OF THE EARTH, INC.] 2 METHYLCHLOROISOTHIAZOLINONE INACTIVE INGREDIENT DEL7T5QRPN FRUIT OF THE EARTH ALOE VERA COOL BLUE (LIDOCAINE HYDROCHLORIDE) GEL [FRUIT OF THE EARTH, INC.] 2 METHYLISOTHIAZOLINONE INACTIVE INGREDIENT 229D0E1QFA FRUIT OF THE EARTH ALOE VERA COOL BLUE (LIDOCAINE HYDROCHLORIDE) GEL [FRUIT OF THE EARTH, INC.] 2 SULISOBENZONE INACTIVE INGREDIENT 1W6L629B4K FRUIT OF THE EARTH ALOE VERA COOL BLUE (LIDOCAINE HYDROCHLORIDE) GEL [FRUIT OF THE EARTH, INC.] 2 TROLAMINE INACTIVE INGREDIENT 9O3K93S3TK FRUIT OF THE EARTH ALOE VERA COOL BLUE (LIDOCAINE HYDROCHLORIDE) GEL [FRUIT OF THE EARTH, INC.] 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 62217-200 FRUIT OF THE EARTH ALOE VERA COOL BLUE (LIDOCAINE HYDROCHLORIDE) GEL [FRUIT OF THE EARTH, INC.] 4 Current NDC, Legacy NDC, 1 package rows 20240725_1d65bc34-2bc2-4f52-a9b3-1cb08324eb79.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 73 of 151 · 3,020 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Nufabrx Lower Leg Sleeve CAPSAICIN Nufabrx LLC b8e3e528-b7cd-e4b7-e053-2995a90a4029 2025-10-15 Warnings Exact identifier application number: M017 Nufabrx Medicine Infused Ankle Sleeve CAPSAICIN Nufabrx LLC 013d60c7-a613-7cdf-e063-6294a90ad584 2025-10-15 Warnings Exact identifier application number: M017 Nufabrx Calf Sleeve CAPSAICIN Nufabrx LLC bd9459c4-5596-746f-e053-2995a90a5400 2025-10-15 Warnings Exact identifier application number: M017 Nufabrx Arm Sleeve CAPSAICIN Nufabrx LLC a7993eaf-6488-a818-e053-2995a90a7ea6 2025-10-15 Warnings Exact identifier application number: M017 Nufabrx Back Wrap CAPSAICIN Nufabrx LLC e4f85ac8-57cb-46eb-e053-2995a90a9b1c 2025-10-15 Warnings Exact identifier application number: M017 Nufabrx Medicine Infused Socks CAPSAICIN Nufabrx LLC 013cb66f-8695-b69f-e063-6294a90a699c 2025-10-15 Warnings Exact identifier application number: M017 Nufabrx Neck Wrap CAPSAICIN Nufabrx LLC e10b420c-500d-5738-e053-2a95a90a008f 2025-10-15 Warnings Exact identifier application number: M017 Nufabrx Knee Sleeve CAPSAICIN Nufabrx LLC a5f455d4-5fc5-d516-e053-2a95a90a921e 2025-10-15 Warnings Exact identifier application number: M017 Nufabrx Medicine Infused Socks CAPSAICIN Nufabrx LLC 00d7d5bf-ee03-e73d-e063-6394a90a5d94 2025-10-15 Warnings Exact identifier application number: M017 Nufabrx Medicine Infused Elbow Sleeve CAPSAICIN Nufabrx LLC 27ef3ef0-2f98-6672-e063-6294a90aeca4 2025-10-15 Warnings Exact identifier application number: M017 Nufabrx Medicine Infused Wrist Sleeve CAPSAICIN Nufabrx LLC 22572cf9-fc0c-d327-e063-6394a90a2186 2025-10-15 Warnings Exact identifier application number: M017 Antibacterial Lidocaine Wound Gel BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE WALGREENS eff77965-dc7f-49af-e053-2995a90a1a97 2025-10-14 Warnings Exact identifier application number: M017 Pleasure Balm Kama Sutra BENZOCAINE Cosmetic Enterprises Ltd f370e3c4-65ca-4f3c-a5aa-70e198e681a2 2025-10-14 Warnings Exact identifier application number: M017 Vanicream HC Anti-Itch HYDROCORTISONE Pharmaceutical Specialties, Inc. 28b06507-27a5-2cb1-e054-00144ff8d46c 2025-10-14 Warnings Exact identifier application number: M017 Trilogel LIDOCAINE HYDROCHLORIDE Trifluent Pharma LLC 22af7d63-6a56-4a38-a95b-0f88410b23cb 2025-10-14 Warnings Exact identifier application number: M017 PROINNATE Numbing Cream MENTHOL Guangzhou Haishi Biological Technology Co., Ltd. 40c63645-8ed3-82b3-e063-6294a90a5267 2025-10-13 Warnings Exact identifier application number: M017 Cramergesic MENTHOL, METHYL SALICYLATE The Hygenic Company, LLC d0ffde7a-6942-74fc-e053-2a95a90a484a 2025-10-13 Warnings Exact identifier application number: M017 Tricylate MENTHOL, UNSPECIFIED FORM AND METHYL SALICYLATE Trifluent Pharma LLC 4869b63a-e01e-4a79-a493-7a1b4d3e914b 2025-10-13 Warnings Exact identifier application number: M017 Doloflex Pain Relief MENTHOL, METHYL SALICYLATE United Health & Beauty Corp 32a830cc-04d3-102e-e063-6294a90a1cad 2025-10-12 Warnings Exact identifier application number: M017 Lidocaine Pain Relieving Gel-Patch LIDOCAINE Nanjing Anxing Medical Technology Co., Ltd. 40c9b132-57ce-865e-e063-6394a90a2080 2025-10-10 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 62217-200-20 62217020020 567 g in 1 BOTTLE (62217-200-20) 567 g 2014-09-10 0000-00-00 No No Current