MyDerm Bite Relief Mediocated Ointment

MyDerm Bite Relief by

Drug Labeling and Warnings

MyDerm Bite Relief by is a Otc medication manufactured, distributed, or labeled by Inspec Solutions LLC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

MYDERM BITE RELIEF- benzocaine ointment 
Inspec Solutions LLC.

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MyDerm Bite Relief Mediocated Ointment

Active Ingredient:

Benzocaine - 5.0%

Benzocaine - 10.0% ............Pain Relief

Temporary relief of pain and itching associated with insect bites

For external use only

When using this product avoid contact with the eye

Stop use and ask a doctor if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Direction Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily.

Children under 2 years of age: consult a physician

Aloe Barbadensis Leaf Extract

Camphor

Chamomilla Recutita (Matricaria) Flower Extract

Diazolidinyl Urea

Disodium EDTA

Eugenia Caryophyllus (Clove) Flower Oil

Hydrocortisone

Inactive Ingredients:

Mentha Piperita (Peppermint) Oil

Menthol

Methylparaben

Olea Europaea (Olive) Fruit Oil

Papain

PEG-2 Stearate

PEG-2 Stearate SE

Polyethylene

Propylene Glycol

Propylparaben

SD Alcohol 40

Water

MYDERM BITE RELIEF 
benzocaine ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72667-019
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5)	BENZOCAINE	5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
PEG-8 DIMETHICONE (UNII: GIA7T764OD)
PEPPERMINT OIL (UNII: AV092KU4JH)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
WATER (UNII: 059QF0KO0R)
PEG-2 STEARATE (UNII: 94YQ11Y95F)
EDETATE DISODIUM (UNII: 7FLD91C86K)
CAMPHOR (NATURAL) (UNII: N20HL7Q941)
MATRICARIA CHAMOMILLA FLOWERING TOP OIL (UNII: SA8AR2W4ER)
CLOVE OIL (UNII: 578389D6D0)
PROPYLENE GLYCOL 1,2-DISTEARATE (UNII: T65PN3O37H)
OLEA EUROPAEA (OLIVE) OIL UNSAPONIFIABLES (UNII: XO45V955LT)
ALOE (UNII: V5VD430YW9)
METHYLPARABEN (UNII: A2I8C7HI9T)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
ALCOHOL (UNII: 3K9958V90M)
MEDIUM DENSITY POLYETHYLENE (UNII: 3W404QE89S)
MENTHOL (UNII: L7T10EIP3A)
HYDROCORTISONE (UNII: WI4X0X7BPJ)

Product Characteristics
Color		Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72667-019-02	50 g in 1 TUBE; Type 0: Not a Combination Product	12/14/2021	12/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	12/14/2021	12/01/2025

Labeler - Inspec Solutions LLC. (081030372)

Establishment
Name	Address	ID/FEI	Business Operations
Inspec Solutions LLC.		081030372	manufacture(72667-019)

Revised: 2/2026

Document Id: 4af344dc-c75c-a66c-e063-6394a90ad3d3

34390-5

Set id: 58b86956-0192-4e93-9ca5-c41df6f9ea19

Version: 3

Effective Time: 20260216