Label: BRAZZERS ANAL DESENSITIZING- lidocaine cream
- NDC Code(s): 83553-001-00
- Packager: Metro Media Ent
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated November 6, 2023
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- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredient
- Use (s)
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Warnings:
For external use only.
Do not use
this product with a mechanical device. Certain persons can develop allergic reactions to ingredients in this product. If the symptom being treated does not subside or if redness, irritation, swelling, pain or other symptoms develop or increase, discontinue use and consult a doctor. Do not apply onto cracked or broken skin.
- Directions
- Other Information:
- Inactive Ingredients:
- Package Labeling:
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INGREDIENTS AND APPEARANCE
BRAZZERS ANAL DESENSITIZING
lidocaine creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83553-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 20 mg in 1 mL Inactive Ingredients Ingredient Name Strength DIMETHICONE (UNII: 92RU3N3Y1O) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) WATER (UNII: 059QF0KO0R) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) HYDROXYACETOPHENONE (UNII: G1L3HT4CMH) XANTHAN GUM (UNII: TTV12P4NEE) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83553-001-00 29.6 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/06/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M015 07/06/2023 Labeler - Metro Media Ent (089682591) Establishment Name Address ID/FEI Business Operations Bath Concept Cosmetics (Dongguan) Co., Ltd 529623933 manufacture(83553-001)