Label: PRESSY TATTOO NUMBING CREAM- numbing cream cream
- NDC Code(s): 83887-008-01
- Packager: Changsha Beiliang E-commerce Co., Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated June 17, 2025
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Use
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Warnings
1. If symptoms worsen or do not improve within 7 days, seek medical advice.
2. Do not exceed the recommended daily dosage without a doctor's instruction.
3. Consult a doctor immediately if bleeding occurs.
4. Do not insert this product into the rectum using fingers or any applicator.
5. Some people may be allergic to the ingredients. Discontinue use and consult a doctor if symptoms persist or worsen, including redness, irritation, swelling, or pain.
Note: Discontinue use and consult a doctor if symptoms persist or worsen, including redness, irritation, swelling, or pain due to possible allergies to product ingredients. - Do not use
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When Using
If symptoms worsen or do not imorove within 7 davs
seek medicaladvice,Do not exceed the recommended daily dosage
Do not insert this product into the rectum using fingers or any applicator
Some peoole mav be aleroic to he inoredients, biscontinwe use and consut a doctor if symotoms persistor worsen including redness irtation swelina or nain
without doctor'sinstruction.Consult a doctor immediately if bleedina occurs - Stop Use
- Ask Doctor
- Keep Out Of Reach Of Children
- Directions
- Other information
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
PRESSY TATTOO NUMBING CREAM
numbing cream creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83887-008 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 5 g in 100 g Inactive Ingredients Ingredient Name Strength DIMETHICONE (UNII: 92RU3N3Y1O) STEARETH-21 (UNII: 53J3F32P58) METHYLPARABEN (UNII: A2I8C7HI9T) MINERAL OIL (UNII: T5L8T28FGP) PETROLATUM (UNII: 4T6H12BN9U) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) STEARETH-2 (UNII: V56DFE46J5) IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB) GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) PROPYLPARABEN (UNII: Z8IX2SC1OH) DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) LAUROCAPRAM (UNII: 1F3X9DRV9X) ALLANTOIN (UNII: 344S277G0Z) AMMONIUM METHACRYLATE (UNII: J2243103QO) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) ROSE OIL (UNII: WUB68Y35M7) .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83887-008-01 60 g in 1 BOTTLE; Type 0: Not a Combination Product 06/12/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 06/12/2025 Labeler - Changsha Beiliang E-commerce Co., Ltd (632138945) Establishment Name Address ID/FEI Business Operations Changsha Beiliang E-commerce Co., Ltd 632138945 label(83887-008) , manufacture(83887-008)

