Label: CREAMOL HAND SANITIZING WIPE- alcohol swab
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Contains inactivated NDC Code(s)
NDC Code(s): 77892-020-01 - Packager: Laber Kimya AR-GE Sanayi Ticaret Levent KAHRIMAN
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated November 18, 2020
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient(s)
- Purpose
- Use
- Warnings
- Do not use
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
- Inactive ingredients
- Package Label - Principal Display Panel
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INGREDIENTS AND APPEARANCE
CREAMOL HAND SANITIZING WIPE
alcohol swabProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:77892-020 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 80 g in 100 g Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) HYPERICUM PERFORATUM WHOLE (UNII: XK4IUX8MNB) MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:77892-020-01 4 g in 1 POUCH; Type 0: Not a Combination Product 11/18/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 11/18/2020 Labeler - Laber Kimya AR-GE Sanayi Ticaret Levent KAHRIMAN (533149962) Establishment Name Address ID/FEI Business Operations Laber Kimya AR-GE Sanayi Ticaret Levent KAHRIMAN 533149962 manufacture(77892-020)