EQUATE CALASPRAY- pramoxine hcl 1%, zinc acetate 0.1% spray

Equate Calaspray by

Drug Labeling and Warnings

Equate Calaspray by is a Otc medication manufactured, distributed, or labeled by Walmart Inc, Derma Care Research Labs. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Pramoxine HCl 1%, Zinc acetate 0.1%

PURPOSE

Topical analgesic / Skin protectant

INDICATIONS & USAGE

For the temporary relief of pain and itching associated with

• rashes due to poison ivy, oak and sumac
• insect bites
• minor skin irritations
• minor cuts
• dries the oozing and weeping of poison ivy, oak, and sumac

WARNINGS

For external use only.

Flammable. Keep away from fire or flame.

Do not use on deep or puncture wounds, animal bites, or serious burns.

When using this product

• avoid contact with eyes. In case of contact with eyes, flush thoroughly with water.
• avoid contact with broken skin,
• do not inhale or ingest,
• contents under pressure. Do not puncture or incinerate. Do not store at temperature above 120F.

Stop use and ask a doctor if condition worsens, rash or irritation develops and lasts for more than 7 days or clears up and occurs again within a few days.

KEEP OUT OF REACH OF CHILDREN

If product is swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

DOSAGE & ADMINISTRATION

Adults and children 2 years or older: apply to affected are not more than 3 to 4 times daily. Children under 2 years of age: ask a doctor. To apply to face, spray into palm of hand and gently apply.

INACTIVE INGREDIENT

Alcohol denat., camphor, citric acid, ethylhexylglycerin, fragrance, glycerin, hydroxypropyl methylcellulose, phenoxyethanol, polysorbate 40, propylene glycol, sodium citrate, water.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

EQUATE CALASPRAY 
pramoxine hcl 1%, zinc acetate 0.1% spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79903-212
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056)	PRAMOXINE HYDROCHLORIDE	1 g  in 100 g
ZINC ACETATE (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37)	ZINC ACETATE	0.1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
PHENOXYETHANOL (UNII: HIE492ZZ3T)
WATER (UNII: 059QF0KO0R)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
ALCOHOL (UNII: 3K9958V90M)
POLYSORBATE 40 (UNII: STI11B5A2X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79903-212-03	85 g in 1 CAN; Type 0: Not a Combination Product	12/26/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	12/26/2023

Labeler - Walmart Inc (051957769)

Registrant - Derma Care Research Labs (116817470)

Establishment
Name	Address	ID/FEI	Business Operations
Derma Care Research Labs		116817470	manufacture(79903-212)