Label: LIDOCAINE DRY- lidocaine spray
- NDC Code(s): 69842-543-04
- Packager: CVS
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 16, 2024
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- Official Label (Printer Friendly)
- Active Ingredient
- Topical Anesthetic
- Use
- Warnings
- Do not use
-
When using this product
- Use only as directed. Read and follow all directions and warnings on this label
- do not allow contact with the eyes and mucous membranes
- avoid spraying on face
- avoid inhalation of spray
- do not bandage or apply local heatl(such as heating pads) or a medicated patch to area of use
- do not use at the same time as other topical analgesics
- Stop use and as a doctor if
- Extremely Flammable
- If pregnant or breast-feeding
- Keep out of reach of children
- Directions
- Inactive Ingredients
- Principal Display Panel
-
INGREDIENTS AND APPEARANCE
LIDOCAINE DRY
lidocaine sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69842-543 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 mL Inactive Ingredients Ingredient Name Strength PROPYLENE GLYCOL (UNII: 6DC9Q167V3) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69842-543-04 113 mL in 1 CAN; Type 0: Not a Combination Product 07/22/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 07/22/2021 Labeler - CVS (062312574)