Label: ALCOHOL PREP PAD- alcohol swab
- NDC Code(s): 59194-002-01
- Packager: Zhejiang Changdi Medical Co., Ltd.
- 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%Close
For preparation of skin prior to an injectionClose
For External use only.
Flammabel,keep away from fire or flame
Do not use
- with electrocautery procedures,
- in the eyes,
stop use if irritation and redness develop.
Ask a doceor if condition persists for more than 72 hours
Keep out of reach of children except with adult supervision.
If swallowed,get medical help or contact a Poison Control Center right away.
wipe injection site vigorously and discard
Other informaiton store at room temperatureClose
- Inactive Ingredients
Inactive Ingredients: WaterClose
- INGREDIENTS AND APPEARANCE
ALCOHOL PREP PAD
isopropyl alcohol swab
Product Information Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:59194-002 Route of Administration TOPICAL DEA Schedule Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (ALCOHOL) ALCOHOL 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength water 30 mL in 100 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59194-002-01 24 in 1 CARTON 1 100 in 1 BOX 1 0.49 mL in 1 POUCH Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 07/02/2013 Labeler - Zhejiang Changdi Medical Co., Ltd. (528198683) Establishment Name Address ID/FEI Business Operations Zhejiang Changdi Medical Co., Ltd. 528198683 manufacture(59194-002)