Home NDC 52412-200 Sting-Kill
Product NDC 52412-200
11-digit product format 524120200
Labeler code 52412
Product ID 52412-200_0dae32b1-8bb5-dcf2-e063-6294a90a3637
Type HUMAN OTC DRUG
Nonproprietary name Benzocaine and Menthol
Dosage form SOLUTION
Route TOPICAL
Labeler RANDOB LABS, LTD. DBA CROSSINGWELL CONSUMER HEALTH
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 1965-01-01
Substance BENZOCAINE; MENTHOL
Active strength 200; 10 mg/mL; 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 · 4 matching rows.
View current auxiliary records. · View the auxiliary file history.
Dataset, Scope, Package NDC table Dataset Scope Package NDC excluded product product excluded package package 52412-200-12 excluded package package 52412-200-10 excluded package package 52412-200-11
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 Sting-Kill
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZOCAINE 200 mg/mL MENTHOL 10 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination U3RSY48JW5 Internal UNII lookup L7T10EIP3A Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1552282 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 52412-200-10 Sting-Kill 0.5 mL in 1 VIAL, SINGLE-USE SOLUTION 0.5 2 52412-200-10 Sting-Kill 5 in 1 BLISTER PACK SOLUTION 5 2 52412-200-11 Sting-Kill 5 in 1 BLISTER PACK SOLUTION 5 2 52412-200-11 Sting-Kill 1 in 1 CARTON SOLUTION 1 2 52412-200-12 Sting-Kill 5 in 1 BLISTER PACK SOLUTION 5 2 52412-200-12 Sting-Kill 2 in 1 CARTON SOLUTION 2 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 52412-200 STING-KILL (BENZOCAINE AND MENTHOL) SOLUTION [RANDOB LABS, LTD. DBA CROSSINGWELL CONSUMER HEALTH] 2 Current NDC, Legacy NDC, 6 package rows 20231230_b8bd9280-f20a-4b2a-aef7-a0ba7b3b8701.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 50 of 152 · 3,029 matching rows.
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 52412-200-10 52412020010 5 VIAL, SINGLE-USE in 1 BLISTER PACK (52412-200-10) / .5 mL in 1 VIAL, SINGLE-USE 1965-01-01 0000-00-00 No No Current 52412-200-11 52412020011 1 BLISTER PACK in 1 CARTON (52412-200-11) / 5 VIAL, SINGLE-USE in 1 BLISTER PACK / .5 mL in 1 VIAL, SINGLE-USE 1 blister pack 2017-01-15 0000-00-00 No No Current 52412-200-12 52412020012 2 BLISTER PACK in 1 CARTON (52412-200-12) / 5 VIAL, SINGLE-USE in 1 BLISTER PACK / .5 mL in 1 VIAL, SINGLE-USE 2 blister pack 1996-01-01 0000-00-00 No No Current