Label: DEEVEEANT NUMB- lidocaine cream
- NDC Code(s): 71383-014-02
- Packager: Valekista Limited
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph 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 July 6, 2017
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredient
- Purpose
- Use
- Warnings
- Directions
- Other information
-
Inactive ingredients
Aloe barbadensis leaf juice, arginine, benzophenone-4, cetyl alcohol, dimethyl sulfoxide, melaleuca alternifolia (tea tree) leaf oil, phenoxyethanol; (and) caprylyl glycol (and) potassium sorbate (and) water (and) hexylene glycol, purified water, simmondsia chinensis (jojoba) seed oil, sodium polyacrylate, stearic acid
- Questions or Comments?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 56 g Tube Box
-
INGREDIENTS AND APPEARANCE
DEEVEEANT NUMB
lidocaine creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71383-014 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Lidocaine (UNII: 98PI200987) (Lidocaine - UNII:98PI200987) Lidocaine 40 mg in 1 g Inactive Ingredients Ingredient Name Strength Aloe Vera Leaf (UNII: ZY81Z83H0X) Arginine (UNII: 94ZLA3W45F) Sulisobenzone (UNII: 1W6L629B4K) Cetyl Alcohol (UNII: 936JST6JCN) Dimethyl Sulfoxide (UNII: YOW8V9698H) Tea Tree Oil (UNII: VIF565UC2G) Phenoxyethanol (UNII: HIE492ZZ3T) Caprylyl Glycol (UNII: 00YIU5438U) Potassium Sorbate (UNII: 1VPU26JZZ4) Hexylene Glycol (UNII: KEH0A3F75J) Water (UNII: 059QF0KO0R) Jojoba Oil (UNII: 724GKU717M) Sodium Polyacrylate (2500000 MW) (UNII: 05I15JNI2J) Stearic Acid (UNII: 4ELV7Z65AP) Product Characteristics Color WHITE Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71383-014-02 1 in 1 BOX 04/30/2017 1 56 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH FINAL part348 04/30/2017 Labeler - Valekista Limited (664452239)