Burn

Product NDC
50332-0209
11-digit product format
503320209
Labeler code
50332
Product ID
50332-0209_8dfa2b7a-8953-4f4b-be02-a28f9a27071e
Type
HUMAN OTC DRUG
Nonproprietary name
Lidocaine
Dosage form
SPRAY
Route
TOPICAL
Labeler
HART Health
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-08-15
Substance
LIDOCAINE HYDROCHLORIDE
Active strength
2 mg/100mL
Pharmacologic classes
Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Burn
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
LIDOCAINE HYDROCHLORIDE2 mg/100mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiV13007Z41A

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
860a93dc-4863-49cc-b284-6bbe8191bc48Product name420250214
9b4cf230-fd05-41d5-98c6-5db9ecb27b86Product name120230117
68ed98f8-24c2-44a0-944a-6d36e82ce25aProduct name120141222
1cd42bc2-a430-c72b-636d-991b235fbf80Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50332-0209-1Burn59 mL in 1 BOTTLE, SPRAYSPRAY591

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
50332-0209-15033202090159 mL in 1 BOTTLE, SPRAY (50332-0209-1) 59 ml2025-08-15NoNoHistorical