133 Medline Retail Nasal Swabs

Medline by

Drug Labeling and Warnings

Medline by is a Otc medication manufactured, distributed, or labeled by Medline Industries, LP. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

MEDLINE- ethyl alcohol swab 
Medline Industries, LP

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133 Medline Retail Nasal Swabs

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 fire or flame.

Do not use

• in the eyes
• on children under 2 years of age unless directed by a doctor

Ask a doctor before use if injuries are

• deep or puncture wounds
• serious burns

Stop use and ask a doctor if

• redness, irritation, swelling or pain persists or increases
• infection occurs

Keep out of reach of children.

If accidentally swallowed, seek medical assistance or immediately contact a Poison Control Center.

Directions

• 1. use a tissue to clean the inside of both nostrils, including the inside tip of nostril. Discard
• 2. insert swab comfortably into tip of right nostril and rotate for 30 seconds, covering all surfaces
• 3. using same swab, repeat step 2 with tip of left nostril
• 4. do not blow nose. If solution drips, gently wipe with a tissue

Other information

• protect from freezing and avoid excessive heat
• not made with natural rubber latex

Inactive ingredients

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

Manufacturing Information

Manufactured by:

Medline Industries, LP

Three Lakes Drive, Northfield, IL 60093 USA

Made in USA

1-800-MEDLINE (633-5463)

REF: MDSR1971

V2 RJ21APL

Package Label

MEDLINE 
ethyl alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53329-133
Route of Administration	TOPICAL

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

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53329-133-27	10 in 1 BOX	01/01/2022	01/31/2025
1	NDC: 53329-133-78	6 mL in 1 PACKET; Type 0: Not a Combination Product
2	NDC: 53329-133-78	6 mL in 1 PACKET; Type 0: Not a Combination Product	01/01/2022	01/31/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	01/01/2022	01/31/2025

Labeler - Medline Industries, LP (025460908)

Registrant - Medline Industries, LP (025460908)

Revised: 11/2023

Document Id: 0b653332-6ea1-bb94-e063-6294a90a24c3

34390-5

Set id: d670cda9-381e-9985-e053-2a95a90a7dc9

Version: 6

Effective Time: 20231130