NDC 69842-731 Bite And Sting Relief Stick

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:
69842-731
Proprietary Name:
Bite And Sting Relief Stick
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Cvs Health
Labeler Code:
69842
Start Marketing Date: [9]
04-17-2020
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 69842-731-01

Package Description: 1 TUBE, WITH APPLICATOR in 1 CARTON / 14.79 g in 1 TUBE, WITH APPLICATOR

Product Details

What is NDC 69842-731?

The NDC code 69842-731 is assigned by the FDA to the product Bite And Sting Relief Stick which is product labeled by Cvs Health. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69842-731-01 1 tube, with applicator in 1 carton / 14.79 g in 1 tube, with applicator. 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 Bite And Sting Relief Stick?

■ Clean area ■ Apply a small amount to the bite area while massaging with sponge tip applicator. If itching persists, apply again in 10-15 minutes ■ For ticks and bees, remove tick or stinger before treatment ■ Adults and children 2 years and over: Apply to affected area 1 to 3 times daily ■ Children under 2 years: Consult a doctor

Which are Bite And Sting Relief Stick UNII Codes?

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

Which are Bite And Sting Relief Stick 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:

What is the NDC to RxNorm Crosswalk for Bite And Sting Relief Stick?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 1435257 - benzocaine 5 % / camphor 3 % / phenol 1.35 % Topical Solution
  • RxCUI: 1435257 - benzocaine 50 MG/ML / camphor 30 MG/ML / phenol 13.5 MG/ML Topical Solution

* Please review the disclaimer below.

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".