Label: ANECREAM- lidocaine 4% cream
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NDC Code(s):
24357-701-01,
24357-701-05,
24357-701-06,
24357-701-07, view more24357-701-15, 24357-701-30, 24357-701-50
- Packager: Focus Health Group
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 12, 2024
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- Official Label (Printer Friendly)
- Active Ingredient:
- Purpose
- Uses
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WARNINGS
For external use only.
When using this product
- do not use in or near the eyes
- do not use in large quantities, particularly over raw surfaces or blistered areas
- Directions
- Other Information
- Inactive ingredients
- Anecream 30g Tube
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INGREDIENTS AND APPEARANCE
ANECREAM
lidocaine 4% creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:24357-701 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 4 g in 100 g Inactive Ingredients Ingredient Name Strength BENZYL ALCOHOL (UNII: LKG8494WBH) WATER (UNII: 059QF0KO0R) CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E) CHOLESTEROL (UNII: 97C5T2UQ7J) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) POLYSORBATE 80 (UNII: 6OZP39ZG8H) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8) TROLAMINE (UNII: 9O3K93S3TK) Product Characteristics Color Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:24357-701-30 1 in 1 CARTON 06/01/2007 1 30 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:24357-701-15 1 in 1 CARTON 06/01/2007 2 15 g in 1 TUBE; Type 0: Not a Combination Product 3 NDC:24357-701-07 5 in 1 CARTON 06/01/2007 3 NDC:24357-701-05 5 g in 1 TUBE; Type 0: Not a Combination Product 4 NDC:24357-701-06 5 in 1 CARTON 03/11/2011 4 NDC:24357-701-05 5 g in 1 TUBE; Type 0: Not a Combination Product 5 NDC:24357-701-50 50 in 1 CARTON 08/01/2020 5 NDC:24357-701-01 2.5 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 06/01/2007 Labeler - Focus Health Group (826939949) Registrant - DSC Laboratories Inc. (097807374) Establishment Name Address ID/FEI Business Operations DSC Laboratories Inc. 097807374 manufacture(24357-701)