GNP Original Anti-Itch Lotion

Manufacturer: AMERISOURCEBERGEN DRUG CORPORATION | Weeks & Leo
Effective date: 2024-12-23
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 00:48:31

Label at a glance#

ProductGNP Anti Itch

Active ingredientMENTHOL, CAMPHOR (SYNTHETIC)

Label structure8 sections

Indications and uses

temporary relieves pain and itching due to: insect bites minor burns sunburn minor skin irritations minor cuts scrapes rashes due to poison ivy, poison oak, and poison sumac

Dosage and administration

to open, squeeze cap tightly and turn pump counter-clockwise adults and children 2 years and older: apply to affected area not more than 3 to 4 times daily children under 2 years: ask a doctor

Storage and handling

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

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Camphor 0.5%............................................................................................................................ External analgesic

Menthol 0.5%.............................................................................................................................. External analgesic

Uses

INDICATIONS & USAGE SECTION

temporary relieves pain and itching due to:

insect bites

minor burns

sunburn

minor skin irritations

minor cuts

scrapes

rashes due to poison ivy, poison oak, and poison sumac

Warning

WARNINGS SECTION

For external use only

Ask doctor before use

OTC - ASK DOCTOR SECTION

on chicken pox

on measles

when using this product

OTC - WHEN USING SECTION

do not get into eyes

Stop Use and ask doctor if

OTC - STOP USE SECTION

condition worsens

symptoms last more than 7 days or clear up and occur again within 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.

Purpose

OTC - PURPOSE SECTION

Anti - itch

Directions

DOSAGE & ADMINISTRATION SECTION

to open, squeeze cap tightly and turn pump counter-clockwise

adults and children 2 years and older: apply to affected area not more than 3 to 4 times daily

children under 2 years: ask a doctor

Other information

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

carbomer 940, cetyl alcohol, DMDM hydantoin, fragrance, glyceryl stearate, isopropyl myristate, PEG-40 stearate, PEG-100 stearate,
purified water, sodium hydroxide, stearic acid, white petrolatum.

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

68-262-75v2.2 back panel68-262-75v2.2 Front panel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
200176	camphor 0.5 % / menthol 0.5 % Topical Lotion	PSN	2
200176	camphor 5 MG/ML / menthol 5 MG/ML Topical Lotion	SCD	2
200176	camphor 0.5 % / menthol 0.5 % Topical Lotion	SY	2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
46122-573-10	GNP Anti Itch	212 g in 1 BOTTLE, PUMP	LOTION	212		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
46122-573	GNP ANTI ITCH (CAMPHOR, MENTHOL) LOTION [AMERISOURCEBERGEN DRUG CORPORATION]	2	Current NDC, Legacy NDC, 1 package rows	20241225_b4f2d6f7-2287-47d8-e053-2995a90ae335.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

GNP Anti Itch
Camphor, Menthol
MENTHOL
MENTHOL, UNSPECIFIED FORM
PEG-40 STEARATE
STEARIC ACID
CARBOMER 940
SODIUM HYDROXIDE
DMDM HYDANTOIN
ISOPROPYL MYRISTATE
CETYL ALCOHOL
PEG-100 STEARATE
GLYCERYL STEARATE SE
CAMPHOR (SYNTHETIC)
PETROLATUM
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
46122-573	46122-573-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
MENTHOL	L7T10EIP3A	ACTIB
PEG-40 STEARATE	ECU18C66Q7	IACT
STEARIC ACID	4ELV7Z65AP	IACT
CARBOMER 940	4Q93RCW27E	IACT
SODIUM HYDROXIDE	55X04QC32I	IACT
DMDM HYDANTOIN	BYR0546TOW	IACT
ISOPROPYL MYRISTATE	0RE8K4LNJS	IACT
CETYL ALCOHOL	936JST6JCN	IACT
PEG-100 STEARATE	YD01N1999R	IACT
GLYCERYL STEARATE SE	FCZ5MH785I	IACT
CAMPHOR (SYNTHETIC)	5TJD82A1ET	ACTIB
PETROLATUM	4T6H12BN9U	IACT
WATER	059QF0KO0R	IACT

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
GNP Anti Itch	CAMPHOR, MENTHOL	AMERISOURCEBERGEN DRUG CORPORATION	b4f2d6f7-2287-47d8-e053-2995a90ae335	2024-12-23	Warnings	Exact identifier ndc (package): 46122-573-10 ndc (product): 46122-573 ndc11 (package): 46122057310 spl id: 29f1d02f-5a14-e708-e063-6294a90a2acf spl set id: b4f2d6f7-2287-47d8-e053-2995a90ae335

Reported adverse events (FAERS/openFDA)#

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