NDC 55636-590

Promescent

Lidicaine

Promescent is a Topical Spray in the Human Otc Drug category. It is labeled and distributed by Absorption. The primary component is Lidocaine.

• Product ID: 55636-590_0f708e60-9a28-402b-b68e-6cb5fceb0202
• NDC: 55636-590
• Product Type: Human Otc Drug
• Proprietary Name: Promescent
• Generic Name: Lidicaine
• Dosage Form: Spray
• Route of Administration: TOPICAL
• Marketing Start Date: 2013-01-11
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part348
• Labeler Name: Absorption
• Substance Name: LIDOCAINE
• Active Ingredient Strength: 10 g/100g
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 55636-590-13

1 BOTTLE, SPRAY in 1 CARTON (55636-590-13) > 1.3 g in 1 BOTTLE, SPRAY

• Marketing Start Date: 2013-01-11
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 55636-590-13 [55636059013]

Promescent SPRAY

• Marketing Category: OTC monograph final
• Application Number: part348
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2013-01-11
• Inactivation Date: 2019-11-27
• Reactivation Date: 2020-03-10

NDC 55636-590-26 [55636059026]

Promescent SPRAY

• Marketing Category: OTC monograph final
• Application Number: part348
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2013-01-11

NDC 55636-590-74 [55636059074]

Promescent SPRAY

• Marketing Category: OTC monograph final
• Application Number: part348
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2013-01-11
• Inactivation Date: 2019-11-27
• Reactivation Date: 2020-03-10

NDC 55636-590-52 [55636059052]

Promescent SPRAY

• Marketing Category: OTC monograph final
• Application Number: part348
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2013-01-11

Drug Details

Active Ingredients

Ingredient	Strength
LIDOCAINE	10 g/100g

OpenFDA Data

• SPL SET ID: 5b508238-3be7-4b0d-bf35-51de79f58f55
• Manufacturer:
  • Absorption
• UNII:
  • 98PI200987