DEEP COVER BUG BITE RELIEF- benzocaine ointment

Deep Cover Bug Bite Relief by

Drug Labeling and Warnings

Deep Cover Bug Bite Relief by is a Otc medication manufactured, distributed, or labeled by Morrisons Outdoors, LLC, Derma Care Research Labs, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Benzocaine 10%

PURPOSE

Pain Relief

DOSAGE & ADMINISTRATION

Uses: for the temporary relief of pain and itching associated with chigger bites, red bug bites, ticks, and mosquito bites.

WARNINGS

For external use only.

When using this product avoid contact with eyes. Stop use and ask a doctor if the condition worsens, symptoms persist for more than 7 days or clear up and occur again within a few days.

KEEP OUT OF REACH OF CHILDREN

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

INDICATIONS & USAGE

Adults and children 2 years and older: apply to the affected area, not more than 3 to 4 times daily. Children under 2 years of age: ask a doctor.

INACTIVE INGREDIENT

Water, PEG-2 Stearate, Olea Europaea (Olive) Fruit Extract, Mentha Piperita (Peppermint) Oil, Aloe Barbadensis Leaf Extract, Camphor, Eugenia Caryophyllus (Clove) Flower Oil, Chamomilla Recutita (Matricaria) Flower Extract, Propylene Glycol, Tocopheryl Acetate, Ascorbic Acid, Retinyl Palmitate, Cholecalciferol, Fragrance, Methylparaben, Propylparaben, Diazolidinyl Urea, Disodium EDTA, Cymbopogon Flexuosus (Lemongrass) Oil,

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DEEP COVER BUG BITE RELIEF 
benzocaine ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84806-147
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5)	BENZOCAINE	10 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
LEMONGRASS OIL (UNII: 5BIA40E9ED)
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
PEG-2 STEARATE (UNII: 94YQ11Y95F)
CLOVE OIL (UNII: 578389D6D0)
MATRICARIA CHAMOMILLA FLOWERING TOP OIL (UNII: SA8AR2W4ER)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PEPPERMINT OIL (UNII: AV092KU4JH)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
EDETATE DISODIUM (UNII: 7FLD91C86K)
ASCORBIC ACID (UNII: PQ6CK8PD0R)
OLIVE OIL (UNII: 6UYK2W1W1E)
METHYLPARABEN (UNII: A2I8C7HI9T)
WATER (UNII: 059QF0KO0R)
CHOLECALCIFEROL (UNII: 1C6V77QF41)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84806-147-03	99 g in 1 JAR; Type 0: Not a Combination Product	07/24/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	07/24/2024

Labeler - Morrisons Outdoors, LLC (031317468)

Registrant - Derma Care Research Labs, LLC (116817470)

Establishment
Name	Address	ID/FEI	Business Operations
Derma Care Research Labs, LLC		116817470	manufacture(84806-147)