Home NDC 70742-287 BODY ACTION PRODUCTS Anal Glide Extra
Product NDC 70742-287
11-digit product format 707420287
Labeler code 70742
Product ID 70742-287_31dee5c7-59d3-d847-e063-6294a90af8ae
Type HUMAN OTC DRUG
Nonproprietary name BENZOCAINE
Dosage form GEL
Route TOPICAL
Labeler PRODUCT MAX GROUP INC
Application M015
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-04-29
Substance BENZOCAINE
Active strength 50 mg/mL
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
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 · 14 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-04-01 02:39 UTC · source 2025-03-31 excluded product product I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 70742-287-00 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 70742-287-00 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 70742-287-00 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 70742-287-00 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 70742-287-00 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 70742-287-00 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 70742-287-00 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…
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 BODY ACTION PRODUCTS Anal Glide Extra
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZOCAINE 50 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination U3RSY48JW5 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2599842 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70742-287-00 BODY ACTION PRODUCTS Anal Glide Extra 60 mL in 1 BOTTLE GEL 60 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70742-287 BODY ACTION PRODUCTS ANAL GLIDE EXTRA (BENZOCAINE) GEL [PRODUCT MAX GROUP INC] 4 Current NDC, Legacy NDC, 1 package rows 20250406_282ac8d3-2caf-42de-b347-450e9c7a9e50.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 1 of 23 · 442 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Flarestop Hemorrhoid Lidocaine LIDOCAINE Chelsea Pharmacceuticals LLC b8a589f7-7131-4807-9bcb-84af3078e258 2026-09-10 Warnings Exact identifier application number: M015 BCBCYC Numbing Cream LIDOCAINE 5% NUMBING CREAM Wenzhou Yuyuan Pharmaceutical Co., Ltd. 5ab36566-ba2f-06ef-e063-6394a90a71b5 2026-09-10 Warnings Exact identifier application number: M015 5% Lidocaine 10g 5% LIDOCAINE Chongqing Mandongzi Technology Co., Ltd 5b10530f-47cd-c4bd-e063-6294a90aaa0a 2026-09-09 Warnings Exact identifier application number: M015 Hemorrhoidal GLYCERIN, PHENYLEPHRINE HCL, PRAMOXINE HCL, WHITE PETROLATUM Rite Aid Corporation 407c78ca-6fee-4ed6-b61b-711ec049c86e 2026-09-09 Warnings Exact identifier application number: M015 Hemorrhoidal GLYCERIN, PHENYLEPHRINE HCL, PRAMOXINE HCL, WHITE PETROLATUM CVS Pharmacy 3167c918-a7d3-46a1-a85b-64f9c22916f2 2026-09-04 Warnings Exact identifier application number: M015 Flushable Hemorrhoidal Medicated Wipes Maximum Strength WITCH HAZEL Amazon.com Services LLC 41d756f3-e523-ed14-e063-6394a90ab817 2026-09-03 Warnings, Adverse reactions Exact identifier application number: M015 Signature Care Medicated Wipes Hemorrhoidal Wipes with Witch Hazel HEMORRHOIDAL WIPES WITH WITCH HAZEL Better Living Brands LLC adf26111-70ba-596c-e053-2995a90ac6f1 2026-09-03 Warnings, Adverse reactions Exact identifier application number: M015 Medicated Wipes Hemorrhoidal Wipes with Witch Hazel WITCH HAZEL CVS Pharmacy, Inc. 1fa7131a-8a94-47f4-826e-197a9cc5ec51 2026-09-03 Warnings, Adverse reactions Exact identifier application number: M015 up and up medicated wipes manixim strength GENTLE HEMORRHOIDAL CARE Target Corporation 271eab2b-ed13-39f1-e054-00144ff88e88 2026-09-03 Warnings, Adverse reactions Exact identifier application number: M015 KROGER MEDICATED WIPES HEMORRHOIDAL WIPE WITH WITCH HAZEL AND ALOE WITCH HAZEL CLOTH The Kroger Co. 48c1598d-6667-446f-ac90-10ab945d0617 2026-09-03 Warnings, Adverse reactions Exact identifier application number: M015 Rexall Medicated WipesHemorrhoidal wipe Hemorrhoidal wipes with witch hazel WITCH HAZEL Old East Main Co. 2055289d-962e-46a9-b371-b5bb93dd46b4 2026-09-03 Warnings, Adverse reactions Exact identifier application number: M015 Equate Hemorrhoidal Medicated Wipes WITCH HAZEL Walmart Inc. 8d57f054-77dc-4205-85f1-b65dcfde677b 2026-09-03 Warnings, Adverse reactions Exact identifier application number: M015 Lidocaine Cream LIDOCAINE InvaDerm Corporation 5a7273d1-1dbc-420e-e063-6294a90a8629 2026-09-01 Warnings Exact identifier application number: M015 Lidocaine Phenylephrine LIDOCAINE PHENYLEPHRINE YYBA CORP 5a72a190-2129-411e-e063-6394a90a08c2 2026-09-01 Warnings Exact identifier application number: M015 INICEI 5% LIDOCAINE Numbing Cream 5% LIDOCAINE NUMBING CREAM Guangzhou Jingliang Cosmetics Co., Ltd. 5a65842f-27a1-268b-e063-6294a90a6054 2026-08-31 Warnings Exact identifier application number: M015 AnievaLC LIDOCAINE Blackstone Products, LLC ddaba14c-10de-44e2-ae13-9217e20cb48e 2026-08-29 Warnings Exact identifier application number: M015 Norms Hemorrhoid Wipes WITCH HAZEL Totally Normal Company 5a1af50b-8d00-f589-e063-6394a90af86c 2026-08-28 Warnings Exact identifier application number: M015 LAIYINHE Numbing Cream Anorectal (Hemorrhoidal) Cream LIDOCAINE Guangzhou Hechuang Commercial Service Co.,Ltd. 59f0fa16-5eb0-e6bb-e063-6294a90aacf5 2026-08-26 Warnings Exact identifier application number: M015 Dude Hemorrhoidal Wipes WITCH HAZEL Dude Products fdf408ef-9392-a812-e053-6394a90a0017 2026-08-25 Warnings Exact identifier application number: M015 Norms Medicated Wipes WITCH HAZEL Totally Normal Company 3a78e109-3f7c-fb19-e063-6394a90ae78e 2026-08-22 Warnings Exact identifier application number: M015
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 70742-287-00 70742028700 60 mL in 1 BOTTLE (70742-287-00) 60 ml 2022-04-29 0000-00-00 No No Current