What is NDC 44224-1103?

44224-1103 is the product NDC for After Bite Advanced (sodium bicarbonate), Sodium bicarbonate .7 g/14g liquid, listed with the FDA by Tender Corporation d/b/a Adventure Ready Brands. It has 2 package NDCs, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

After Bite Advanced (Sodium Bicarbonate).

Tender Corporation d/b/a Adventure Ready Brands, NDC labeler code 44224. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for After Bite Advanced?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

After Bite Advanced NDC 44224-1103

NDC codes

FDA NDC Directory

Product NDC (as listed)44224-1103Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44224-1103Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
44224-1103-2	4422411030244224110302	1 VIAL in 1 BOX (44224-1103-2) / 1 g in 1 VIAL (44224-1103-0)Marketed from Jun 17, 2025
44224-1103-3	4422411030344224110303	3 VIAL in 1 BOX (44224-1103-3) / 14 g in 1 VIALMarketed from Dec 18, 2025

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): After Bite Advanced
Generic name (nonproprietary): sodium bicarbonate
Active ingredients: Sodium bicarbonate — .7 g/14g
Dosage form: Liquid
Route: Topical
Labeler: Tender Corporation d/b/a Adventure Ready BrandsNDC labeler code 44224
Product type: Over-the-counter drug
Marketing category: OTC monograph drugApplication M 016
Marketing start: Jun 17, 2025
Listing expires: Dec 31, 2026
Other FDA classes: Alkalinizing Activity (Mechanism)
Identifiers: Product ID 44224-1103_4640051b-84fe-66c7-e063-6294a90a552eSPL ID 4640051b-84fe-66c7-e063-6294a90a552eSPL set ID 223d1de8-7940-bbdc-e063-6294a90a51d8RxCUI 1547234UNII 8MDF5V39QOUPC 0044224610300

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N444224110302 followed by a unit qualifier and the quantity

Package 44224-1103-02. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Dec 18, 2025.

Indications (excerpt from the label)

Uses Temproarily protects and helps relieve minor skin irritation and itching due to insect bite poison ivy, oak sumac

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 44224-1103

What is NDC 44224-1103?: 44224-1103 is the product NDC for After Bite Advanced (sodium bicarbonate), Sodium bicarbonate .7 g/14g liquid, listed with the FDA by Tender Corporation d/b/a Adventure Ready Brands. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: After Bite Advanced (Sodium Bicarbonate).
What is the active ingredient?: Sodium bicarbonate.
Who is the labeler?: Tender Corporation d/b/a Adventure Ready Brands, NDC labeler code 44224. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for After Bite Advanced?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other NDCs under M 016

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under M 016
Product	Strength	Form · route	Labeler	Product NDC
2-Pack Facial Serum	Water 78.894 g/100mL + 4 more ingredients	LiquidCutaneous	Guangzhou Ariel Biotech Co., Ltd.	84148-011
2-Pack Facial Serum	3-o-ethyl ascorbic acid .5 g/100mL + 3 more ingredients	LiquidCutaneous	Guangzhou Ariel Biotech Co., Ltd.	84148-012
3M Cavilon Durable Barrierdimethicone	Dimethicone 13000 mg/L	CreamTopical	Solventum US LLC	17518-030
4% 10gTATTOO Numb Cream4% lidocaine	Lidocaine 100 mg/g	CreamCutaneous	Shengnan (Guangzhou) Cosmetics Co., LTD	84019-031
4% TATTOO Numb Cream4% lidocaine	Lidocaine 100 mg/g	CreamCutaneous	Shengnan (Guangzhou) Cosmetics Co., LTD	84019-030
456 Acne Relief Creamniacinamide,salicylic acid,centella asiatica root,coptis chinensis root	Salicylic acid 380 mg/50g + 3 more ingredients	CreamTopical	Guangzhou Senmai Biotechnology Co.,Ltd.	84509-111
5% Dr.care Numb creamlidocaine	Lidocaine 100 mg/g	CreamCutaneous	Shengnan (Guangzhou) Cosmetics Co., LTD	84019-028
5% Minoxidil	Minoxidil 2 g/100g + 3 more ingredients	SprayCutaneous	Guangzhou Yanxi Biotechnology Co., Ltd	84025-328
5% Minoxidil	Minoxidil 2 g/100g + 3 more ingredients	SprayCutaneous	Guangzhou Yanxi Biotechnology Co., Ltd	84025-329
5% Minoxidil	Biotin .05 g/100g; Niacinamide 2.5 g/100g	SprayCutaneous	Guangzhou Yanxi Biotechnology Co., Ltd	84025-335
5% Minoxidil	Minoxidil 5 g/100g + 5 more ingredients	SprayCutaneous	Guangzhou Yanxi Biotechnology Co., Ltd	84025-337
5% Minoxidil for Men and Women	Biotin .05 g/100g; Tocopherol .05 g/100g	SprayCutaneous	Guangzhou Yanxi Biotechnology Co., Ltd	84025-332
5% Minoxidil Hair Growth	Biotin .1 g/100g + 3 more ingredients	SprayCutaneous	Guangzhou Yanxi Biotechnology Co., Ltd	84025-333
5% Minoxidil Hair Growth	Minoxidil 5 g/100g + 3 more ingredients	SprayCutaneous	Guangzhou Yanxi Biotechnology Co., Ltd	84025-334
5% Signature Numb creamlidocaine	Lidocaine 100 mg/g	CreamCutaneous	Shengnan (Guangzhou) Cosmetics Co., LTD	84019-026
5% Signature Numb cream5% signature	Lidocaine 100 mg/g	CreamCutaneous	Shengnan (Guangzhou) Cosmetics Co., LTD	84019-027
5% Signature Numb cream5% lidocaine	Lidocaine 100 mg/g	CreamCutaneous	Shengnan (Guangzhou) Cosmetics Co., LTD	84019-029
70% Isopropyl Rubbing Alcoholisopropyl alcohol	Isopropyl alcohol 70 mL/100mL	LiquidTopical	MY IMPORTS USA LLC	51628-4501
911allantoin	Allantoin .5 g/100g	OintmentTopical	Skinfix, Inc.	61328-120
A and Dpetrolatum	Petrolatum 76 g/100g	OintmentTopical	Safetec of America, Inc.	61010-4405

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After Bite Advanced (Sodium bicarbonate) NDC 44224-1103