Benadryl Extra Strength Itch Cooling Spray
NDC Package 69968-0270-2
Package Information
Benadryl Extra Strength Itch Cooling (diphenhydramine hydrochloride and zinc acetate) sprays is do not use more than directedadults and children 2 years of age and older: spray on affected area not more than 3 to 4 times dailychildren under 2 years of age: ask a doctor. This formulation utilizes a spray delivery system. Marketed by Kenvue Brands Llc, this product is identified by NDC 69968-0270 and is authorized under FDA application M017.
Identification & Billing
- RxCUI: 1053138 - diphenhydrAMINE HCl 2 % / zinc acetate 0.1 % Topical Spray
- RxCUI: 1053138 - diphenhydramine hydrochloride 20 MG/ML / zinc acetate 1 MG/ML Topical Spray
- RxCUI: 1053138 - diphenhydramine hydrochloride 2 % / zinc acetate 0.1 % Topical Spray
- RxCUI: 1294592 - Benadryl ITCH COOLING 2 % / 0.1 % Topical Spray
- RxCUI: 1294592 - diphenhydramine hydrochloride 20 MG/ML / zinc acetate 1 MG/ML Topical Spray [Benadryl Itch Stopping]
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 69968 - Kenvue Brands Llc
- 69968-0270 - Benadryl Extra Strength Itch Cooling
- 69968-0270-2 - 59 mL in 1 BOTTLE, SPRAY
- 69968-0270 - Benadryl Extra Strength Itch Cooling
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 69968-0270-2 identifies a specific commercial package of 59 ml in 1 bottle, spray of Benadryl Extra Strength Itch Cooling, a human over the counter drug labeled by Kenvue Brands Llc. This product is billed per "ML" milliliter and contains an estimated amount of 59 billable units per package. This spray is formulated for topical use and contains diphenhydramine hydrochloride; zinc acetate as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Kenvue Brands Llc on April 01, 2019. The current certification is valid through December 31, 2026.
How is this Kenvue Brands Llc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 69968027002. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. There are 59 total billable units per package. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Package segment to maintain the 5-4-2 structure.