Target Calamine Plus Spray

Manufacturer: Target Corporation
Effective date: 2024-12-11
Label type: HUMAN OTC DRUG LABEL
Version: 8
Source: legacy-cache
Hydrated at: 2026-08-01 20:46:52

Label at a glance#

ProductCalamine Plus Pramoxine HCl

Active ingredientFERRIC OXIDE RED, ZINC OXIDE, PRAMOXINE HYDROCHLORIDE

Label structure9 sections

Indications and uses

temporarily relieves pain and itching associated with: insect bites rashes minor skin irritations minor cuts dries the oozing and weeping of poison ivy, poison oak and poison sumac

Dosage and administration

shake well before using adults and children 2 years of age and older: apply as needed to the affected area, not more than 3 or 4 times daily cleanse the skin with soap and water let dry before use children under 2 years of age: consult a doctor

Contacts and useful links#

PhoneLabel contact1-866-964-0939

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Calamine 8%
Pramoxine HCl 1%

Purpose

OTC - PURPOSE SECTION

Skin protectant
External analgesic

Uses

INDICATIONS & USAGE SECTION

temporarily relieves pain and itching associated with:

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

Warnings

WARNINGS SECTION

For external use only. Use only as directed. Intentional misuse by deliberately concentrating and inhailing contents can be harmful or fatal.

Flammable:

OTHER SAFETY INFORMATION

Do not use while smoking or near heat or flame. Do not puncture or incinerate. Contents under pressure. Do not store at temperatures above 120°F.

When using this product

OTC - WHEN USING SECTION

do not get into eyes
ask a doctor before using on children under 2 years of age

Stop use and ask a doctor if

OTC - STOP USE SECTION

conditions worsens
symtomps last more than 7 days or clear up and occur again in a few days

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

shake well before using
adults and children 2 years of age and older: apply as needed to the affected area, not more than 3 or 4 times daily
cleanse the skin with soap and water
let dry before use
children under 2 years of age: consult a doctor

Other information

OTHER SAFETY INFORMATION

store between 20° to 25°C (68° to 77°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

benzyl alcohol, camphor, disteardimonium hectorite, fragrance, hydrated silica, isobutane, oleyl alcohol, SD alcohol 40-B, sorbitan trioleate

Questions?

OTC - QUESTIONS SECTION

Call 1-866-964-0939

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

no-rub

calamine

plus spray

Calamine 8% / skin protectant

Promoxine HCL 1% / external analgesic

relieves itching from

poison ivy, oak & sumac, & insect bites

soothes minor

skin irritations

& cuts

NET WT 4.1 OZ(116 g)

Image 1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
11673-635-41	2023-01-31	C162847	48780-1	f386c649-d0fe-0266-e053-dadaa90a7c1a	Target Calamine Plus Spray
11673-635-41	2023-01-30	C162847	48780-1	f386c649-d0fe-0266-e053-dadaa90a7c1a	Target Calamine Plus Spray

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
11673-635	CALAMINE PLUS PRAMOXINE HCL (CALAMINE PLUS SPRAY) AEROSOL, SPRAY [TARGET CORPORATION]	8	Legacy NDC	20241213_9e0174a0-ddd2-4996-9c8c-f5977fd360e2.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 15 matching rows.

Calamine Plus Pramoxine HCl
Calamine Plus Spray
BENZYL ALCOHOL
CAMPHOR (SYNTHETIC)
HYDRATED SILICA
ISOBUTANE
OLEYL ALCOHOL
SORBITAN TRIOLEATE
DISTEARDIMONIUM HECTORITE
ALCOHOL
FERRIC OXIDE RED
ZINC OXIDE
ZINC CATION
PRAMOXINE HYDROCHLORIDE
PRAMOXINE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
11673-635	11673-635-41

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
BENZYL ALCOHOL	LKG8494WBH	IACT
CAMPHOR (SYNTHETIC)	5TJD82A1ET	IACT
HYDRATED SILICA	Y6O7T4G8P9	IACT
ISOBUTANE	BXR49TP611	IACT
OLEYL ALCOHOL	172F2WN8DV	IACT
SORBITAN TRIOLEATE	QE6F49RPJ1	IACT
DISTEARDIMONIUM HECTORITE	X687XDK09L	IACT
ALCOHOL	3K9958V90M	IACT
FERRIC OXIDE RED	1K09F3G675	ACTIB
ZINC OXIDE	SOI2LOH54Z	ACTIM
PRAMOXINE HYDROCHLORIDE	88AYB867L5	ACTIB

Source Document#

Source XML

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
37c71135-55a4-a4aa-e063-6294a90adfc3			9e0174a0-ddd2-4996-9c8c-f5977fd360e2	2025-06-17	Warnings	Exact identifier spl set id: 9e0174a0-ddd2-4996-9c8c-f5977fd360e2

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.