NDC 73000-226 Aopar Water Based Personal Lubricant

Personal Lubricant

NDC Product Code 73000-226

NDC CODE: 73000-226

Proprietary Name: Aopar Water Based Personal Lubricant What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Personal Lubricant What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

Product Characteristics

Color(s):
WHITE (C48325)
Shape: FREEFORM (C48340)
Size(s):
50 MM
Score: 1
Flavor(s):
MINT (C73404)

NDC Code Structure

  • 73000 - Shenzhen Zhihuichuangxiang Technology Co., Ltd
    • 73000-226 - Aopar Water Based Personal Lubricant

NDC 73000-226-20

Package Description: 30 mL in 1 BOTTLE

NDC Product Information

Aopar Water Based Personal Lubricant with NDC 73000-226 is a a human over the counter drug product labeled by Shenzhen Zhihuichuangxiang Technology Co., Ltd. The generic name of Aopar Water Based Personal Lubricant is personal lubricant. The product's dosage form is lotion and is administered via rectal; vaginal form.

Labeler Name: Shenzhen Zhihuichuangxiang Technology Co., Ltd

Dosage Form: Lotion - An emulsion, liquid1 dosage form. This dosage form is generally for external application to the skin.2

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Aopar Water Based Personal Lubricant Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • HYDROXYETHYL CELLULOSE (140 CPS AT 5%) .381 g/30mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • SODIUM BENZOATE (UNII: OJ245FE5EU)
  • WATER (UNII: 059QF0KO0R)
  • POLYSORBATE 20 (UNII: 7T1F30V5YH)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • LACTIC ACID, DL- (UNII: 3B8D35Y7S4)
  • EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Rectal - Administration to the rectum.
  • Vaginal - Administration into the vagina.

Product Labeler Information

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

Labeler Name: Shenzhen Zhihuichuangxiang Technology Co., Ltd
Labeler Code: 73000
Marketing Category: UNAPPROVED DRUG OTHER - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 04-13-2021 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2022 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.

Exclude Flag: N - NO 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".

* Please review the disclaimer below.

Aopar Water Based Personal Lubricant Product Label Images

Aopar Water Based Personal Lubricant Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredient

Hydroxyethyl Cellulose 1.27% w/w

Inactive Ingredient

De-lonized Water, Glycerin, Propylene Glycol, Sodium Benzoate, Polysorbate 20, Disodium EDTA, Lactic Acid

Indication For Use

Aopar Water-based Personal Lubricant is a supplement for the nature lubrication of penis or vagina, intending to moisturize and enhance the ease and comfort of intimate sexual activity.This product is compatible with natural rubber latex, polyurethane and polyisoprene condoms.

When Using

Virginal / Anal dryness and/or intimate sexual activity.This product is not a contraceptive and does not contain a spermicide.

Do Not Use

This product is not a contraceptive or spermicide.

Stop Use

If irriation or discomfor occurs, please discontinue to use and consult a physician. Very slippery surfaces, clean the spills immediately.

Ask Doctor

If irriation or discomfor occurs, please discontinue to use and consult a doctor/physician.

Ask Doctor/Pharmacist

If irriation or discomfor occurs, please discontinue to use and consult a doctor/physician.

Keep Out Of Reach Of Children

Keep out of children and pets' reach.

Questions

Please contact us when you have any questions.86-755-83286325 / [email protected]

Pregnancy Or Breast Feeding

Pregnant or breast feeding women shall follow doctor advice.

Indications & Usage

Aopar Water-based Personal Lubricant is a supplement for the nature lubrication of penis or vagina, intending to moisturize and enhance the ease and comfort of intimate sexual activity.This product is compatible with natural rubber latex, polyurethane and polyisoprene condoms. This product is not a contraceptive or spermicide.

Direction

Apply a small amount to genital areas. Reapply as needed or desired.

Dosage Forms & Strengths

The lubricant is like oil form.The active ingredient strength is 1.27% w/w.

Warnings

If irriation or discomfor occurs, please discontinue to use and consult a physician. Very slippery surfaces, clean the spills immediately. This product is not a contraceptive or spermicide. Keep out of children and pets' reach.

* Please review the disclaimer below.