Label: WALGREEN ALCOHOL- isopropyl alcohol swab
- NDC Code(s): 0363-0809-30, 0363-0809-60, 0363-0809-67
- Packager: Walgreen Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
NOTE: Most over the counter (OTC) are not reviewed and approved by the FDA. However, they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
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- Active ingredient
Isopropyl alcohol, 70% v/vClose
- for preparation of the skin prior to injection
For external use only.
Flammable, keep away from fire or flame.
Stop use and ask a doctor if
- irritation and redness develop
- condition persists for more than 72 hours
Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.
Wipe injection site vigorously and discardClose
- Other information
Protect from freezing. Avoid excessive heat.Close
- Inactive ingredients
- Package/Label Principal Display Panel
Alcohol Prep Pads
Isopropyl Alcohol 70%
Antiseptic for preparation of the skin prior to injection
200 INDIVIDUAL FOIL PACKETS
200 Individual Foil Packets
1.1 IN X 1.33 IN (2.8 cm x 3.4 cm)Close
- Package/Label Back
- INGREDIENTS AND APPEARANCE
isopropyl alcohol swab
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0809 Route of Administration TOPICAL DEA Schedule Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-0809-30 100 in 1 BOX 1 1 in 1 PACKET 1 5 mL in 1 APPLICATOR 2 NDC:0363-0809-67 120 in 1 BOX 2 1 in 1 PACKET 2 5 mL in 1 APPLICATOR 3 NDC:0363-0809-60 200 in 1 BOX 3 1 in 1 PACKET 3 5 mL in 1 APPLICATOR Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 01/01/2011 Labeler - Walgreen Company (008965063)