STING RELIEF PAD- ethyl alcohol, lidocaine swab NOX-A-STING- ethyl alcohol, lidocaine swab

Nox-A-Sting by

Drug Labeling and Warnings

Nox-A-Sting by is a Otc medication manufactured, distributed, or labeled by Honeywell Safety Products USA, Inc, Safetec of America, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

in each wipe:

Ethyl alcohol 50.0%

Lidocaine HCl 2.0%

Purpose

Antiseptic

Topical pain relief

Uses

• prevent infection in minor scrapes, and temporary relief of itching of insect bites

Warnings

• For external use only
• Flammable, keep away from open fire or flame

Do not use

• over large areas of the body
• in eyes
• over raw or blistered areas

Stop use and ask a doctor

• if conditions worsen or 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.

DIRECTIONS

• adults and children 2 years and older: Apply to cleaned affected area not more than 3 times daily.
• children under 2 years of age: consult a doctor.

Inactive ingredients

benzalkonium chloride, menthol, and purified water

Questions or comments?

1-800-430-5490

Sting Relief label

Nox-A-Sting label

INGREDIENTS AND APPEARANCE

STING RELIEF PAD 
ethyl alcohol, lidocaine swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0498-0733
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE HYDROCHLORIDE ANHYDROUS	20 mg  in 1 mL
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.5 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
MENTHOL (UNII: L7T10EIP3A)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0498-0733-00	0.4 mL in 1 POUCH; Type 0: Not a Combination Product	12/23/2017
2	NDC: 0498-0733-34	10 in 1 BOX	12/23/2017
2		0.4 mL in 1 POUCH; Type 0: Not a Combination Product
3	NDC: 0498-0733-10	100 in 1 BOX	12/23/2017
3	NDC: 0498-0733-00	0.4 mL in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	12/23/2017

NOX-A-STING 
ethyl alcohol, lidocaine swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0498-1733
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE HYDROCHLORIDE ANHYDROUS	20 mg  in 1 mL
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.5 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
MENTHOL (UNII: L7T10EIP3A)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0498-1733-34	10 in 1 BOX	12/23/2017
1		0.4 mL in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	12/23/2017

Labeler - Honeywell Safety Products USA, Inc (079287321)

Registrant - Honeywell Safety Products USA, Inc (079287321)

Establishment
Name	Address	ID/FEI	Business Operations
Honeywell Safety Products USA, Inc		079287321	pack(0498-0733, 0498-1733)

Establishment
Name	Address	ID/FEI	Business Operations
Safetec of America, Inc.		874965262	manufacture(0498-0733, 0498-1733)