62% ETHYL ALCOHOL NASAL SWAB- ethyl alcohol nasal swab swab

62% Ethyl Alcohol Nasal Swab by

Drug Labeling and Warnings

62% Ethyl Alcohol Nasal Swab by is a Otc medication manufactured, distributed, or labeled by IIMED MEDICAL MEXICANA S DE RL DE CV. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Ethyl alcohol 62% v/v

Purpose

Antiseptic

Uses

helps reduce bacteria that can cause skin infections

Warnings

For external use only.

flammable, keep away from open flame.

Do not use

-in the eyes

-on children under 2 years of age unless directed by a doctor

Ask doctor before use if injuries are

-deep or puncture wounds

-serious burns

Stop use and ask doctor if

-redness, irritation, swelling or pain persists or increase

-infection occurs

Keep out of reach of children

In case of accidental ingestion, seek professional assistance or consult a poison control center immediately.

Directions

Nasal Application:

1. Use a tissue to clean inside both nostrils, including inside tip of nostil. Discard.

2. Insert right swab comfortable into right nostil and rotate for 30 seconds, covering all surfaces. Discard swab.

3. Using left swab repeat Step 2 with left nostril.

4. Do not blow nose. If solution drips, gently wipe with a tissue.

Other Information

-Store at room temperature

-not made with natural rubber latex

-for hospital or professional use only

Inactive ingredients

ascorbyl palmitate, benzyl alcohol, BHT, castor (ricinus communis) oil, isopropyl alcohol, fragrance, menthol, polyaminopropyl biguanide, purified water

Label

INGREDIENTS AND APPEARANCE

62% ETHYL ALCOHOL NASAL SWAB 
ethyl alcohol nasal swab swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83062-032(NDC:53329-032)
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DEHYDRATED ALCOHOL (UNII: 3K9958V90M) (DEHYDRATED ALCOHOL - UNII:3K9958V90M)	DEHYDRATED ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302)
CASTOR OIL (UNII: D5340Y2I9G)
WATER (UNII: 059QF0KO0R)
POLYAMINOPROPYL BIGUANIDE (UNII: DT9D8Z79ET)
ASCORBYL PALMITATE (UNII: QN83US2B0N)
MENTHOL (UNII: L7T10EIP3A)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
BENZYL ALCOHOL (UNII: LKG8494WBH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83062-032-29	50 mL in 1 PACKET; Type 0: Not a Combination Product	10/15/2023	10/16/2023
2	NDC: 83062-032-78	6 mL in 1 PACKET; Type 0: Not a Combination Product	10/15/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	10/15/2023

Labeler - IIMED MEDICAL MEXICANA S DE RL DE CV (812894376)

Establishment
Name	Address	ID/FEI	Business Operations
IIMED MEDICAL MEXICANA S DE RL DE CV		812894376	repack(83062-032) , relabel(83062-032)