Zicam Cold Remedy Spray
NDC Package 10237-474-15
Package Information
Zicam Cold Remedy (galphimia glauca flowering top, luffa operculata fruit, and schoenocaulon officinale seed) sprays is for best results, use at the first sign of a cold and continue to use until symptoms completely subsideadults and children 12 years of age and older: remove cap and safety cliphold with thumb at bottom of bottle and nozzle between your fingersbefore using the first time, prime pump by depressing several timesplace tip of nozzle just past nasal opening (approximately 1/8")lean your head backwards slightlypump 2 times into each nostrilavoid inhaling deeplywipe away any excessdose every 3 hours, not to exceed 5 doses in one 24 hour periodchildren under 12 years of age: do not use. This formulation utilizes a spray delivery system. Marketed by Church & Dwight Co., Inc., this product is identified by NDC 10237-474.
Identification & Billing
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 10237 - Church & Dwight Co., Inc.
- 10237-474 - Zicam Cold Remedy
- 10237-474-15 - 1 BOTTLE, PLASTIC in 1 CARTON / 15 mL in 1 BOTTLE, PLASTIC
- 10237-474 - Zicam Cold Remedy
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 10237-474-15 identifies a specific commercial package of 1 bottle, plastic in 1 carton / 15 ml in 1 bottle, plastic of Zicam Cold Remedy, a human over the counter drug labeled by Church & Dwight Co., Inc.. This spray is formulated for nasal use and contains galphimia glauca flowering top; luffa operculata fruit; schoenocaulon officinale seed 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 Church & Dwight Co., Inc. on April 10, 2022. The current certification is valid through December 31, 2026.
How is this Church & Dwight Co., Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 10237047415. 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 Product segment to maintain the 5-4-2 structure.