NDC 71847-2215 Water-based Personal Lubricant, Acvioo 001

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
71847-2215
Proprietary Name:
Water-based Personal Lubricant, Acvioo 001
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Shenzhen Dikailong Technology Ltd
Labeler Code:
71847
Start Marketing Date: [9]
10-30-2017
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
BROWN (C48332)

Product Packages

NDC Code 71847-2215-5

Package Description: 240 mL in 1 BOTTLE

NDC Code 71847-2215-7

Package Description: 400 mL in 1 BOTTLE

Product Details

What is NDC 71847-2215?

The NDC code 71847-2215 is assigned by the FDA to the product Water-based Personal Lubricant, Acvioo 001 which is product labeled by Shenzhen Dikailong Technology Ltd. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 71847-2215-5 240 ml in 1 bottle , 71847-2215-7 400 ml in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Water-based Personal Lubricant, Acvioo 001?

ACVIOO 001 is a water-based personal lubricant, for penile and/or vaginal application, intended to lubricate and moisturize, to enhance the ease and comfort of intimate sexual activity, help relieve virginal dryness, and supplement to the body's natural lubricant.Apply a small amount to genital areas. Reapply as needed or desired.

Which are Water-based Personal Lubricant, Acvioo 001 UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Water-based Personal Lubricant, Acvioo 001 Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".