Home NDC 73635-7101-5 Anesgerm LA MUELA
Product NDC 73635-7101
Requested package NDC 73635-7101-5
11-digit product format 736357101
Labeler code 73635
Product ID 73635-7101_5d6d9fe0-9a4b-6ec9-e063-6394a90ab36a
Type HUMAN OTC DRUG
Nonproprietary name Benzocaine 20%
Dosage form LIQUID
Route TOPICAL
Labeler Germa Products, LLC
Application M022
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-03-29
Substance BENZOCAINE
Active strength 200 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 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 · 12 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…
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 Anesgerm LA MUELA
Brand name suffix Fast Pain Relief
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZOCAINE 200 mg/mL
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 73635-7101-5 Anesgerm LA MUELAFast Pain Relief 14.8 mL in 1 BOTTLE, WITH APPLICATOR LIQUID 14.8 6 73635-7101-5 Anesgerm LA MUELAFast Pain Relief 1 in 1 BOX LIQUID 1 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 73635-7101 ANESGERM LA MUELA FAST PAIN RELIEF (BENZOCAINE 20%) LIQUID [GERMA PRODUCTS, LLC] 4 Current NDC, Legacy NDC, 2 package rows 20241017_bf7842a2-9c0b-3fc3-e053-2995a90a36c1.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 9 of 40 · 786 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 73635-7101-5 73635710105 1 BOTTLE, WITH APPLICATOR in 1 BOX (73635-7101-5) / 14.8 mL in 1 BOTTLE, WITH APPLICATOR 2019-03-29 0000-00-00 No No Current