What is NDC 74458-238?

74458-238 is the product NDC for Lyophilized Amnion With Albumin (human amniotic membrane), Human amniotic membrane 2 mg/100mg powder, for solution, listed with the FDA by Guangzhou Yilong Cosmetics.,Ltd. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Lyophilized Amnion With Albumin (Human amniotic membrane).

Guangzhou Yilong Cosmetics.,Ltd, NDC labeler code 74458. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Lyophilized Amnion With Albumin?

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.

Lyophilized Amnion With Albumin NDC 74458-238

NDC codes

FDA NDC Directory

Product NDC (as listed)74458-238Labeler and product segments. Claims need a package NDC.

Product NDC at billing width74458-0238Add 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
74458-238-01	74458023801	10 mg in 1 BOTTLE (74458-238-01)Marketed from Jul 30, 2026

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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): Lyophilized Amnion With Albumin
Generic name (nonproprietary): human amniotic membrane
Active ingredients: Human amniotic membrane — 2 mg/100mg
Dosage form: Powder, For solution
Route: Topical
Labeler: Guangzhou Yilong Cosmetics.,LtdNDC labeler code 74458
Product type: Over-the-counter drug
Marketing category: OTC monograph drugApplication M 001
Marketing start: Jul 11, 2026
Listing expires: Dec 31, 2027
Identifiers: Product ID 74458-238_580de9cc-bae7-fb1b-e063-6394a90ad74cSPL ID 580de9cc-bae7-fb1b-e063-6394a90ad74cSPL set ID 57c5a5a5-bbd1-27c3-e063-6294a90a7453UNII T9O10FB50M

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

N474458023801 followed by a unit qualifier and the quantity

Package 74458-0238-01. 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 Aug 2, 2026.

Indications (excerpt from the label)

Uses: temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: sneezing runny nose itchy, watery eyes itchy throat

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 74458-238

What is NDC 74458-238?: 74458-238 is the product NDC for Lyophilized Amnion With Albumin (human amniotic membrane), Human amniotic membrane 2 mg/100mg powder, for solution, listed with the FDA by Guangzhou Yilong Cosmetics.,Ltd. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Lyophilized Amnion With Albumin (Human amniotic membrane).
What is the active ingredient?: Human amniotic membrane.
Who is the labeler?: Guangzhou Yilong Cosmetics.,Ltd, NDC labeler code 74458. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Lyophilized Amnion With Albumin?: 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 001

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

FDA NDC Directory listings under M 001
Product	Strength	Form · route	Labeler	Product NDC
Acid Gone Antacidaluminum hydroxide and magnesium carbonate	Aluminum hydroxide 95 mg/15mL; Magnesium carbonate 358 mg/15mL	LiquidOral	Major Pharmaceuticals	0904-7727
Acid Gone Antacid Extra Strengthaluminum hydroxide and magnesium carbonate	Aluminum hydroxide 160 mg/1; Magnesium carbonate 105 mg/1	Tablet, ChewableOral	Major Pharmaceuticals	0904-5365
ADRIAN BICARBONATO SODIUM BICARBONATE USP-4 oz, 8 oz and 16 ozsodium bicarbonate	Sodium bicarbonate 315 mg/g	PowderOral	Evi Labs	84178-106
Advanced Antacid Mintaluminum hydroxide, magnesium hydroxide, dimethicone	Aluminum hydroxide 400 mg/10mL + 2 more ingredients	SuspensionOral	GOODSENSE	50804-639
Advanced Regular Strength Antacidaluminum hydroxide, magnesium hydroxide, simethicone	Aluminum hydroxide 200 mg/5mL + 2 more ingredients	SuspensionOral	WALGREEN COMPANY	0363-1639
Alka-Seltzer Cool Action Extra Strength ReliefChews Mintcalcium carbonate	Calcium carbonate 750 mg/1	Tablet, ChewableOral	Bayer HealthCare LLC.	0280-0058
Alka-Seltzer Cool Action Heartburn Relief Mintcalcium carbonate	Calcium carbonate 750 mg/1	Gum, ChewingOral	Bayer HealthCare LLC.	0280-0001
Alka-Seltzer Extra Strengthanhydrous citric acid, sodium bicarbonate, and aspirin	Anhydrous citric acid 1000 mg/1 + 2 more ingredients	Granule, EffervescentOral	Bayer HealthCare LLC.	0280-0211
Alka-Seltzer Extra Strength Heartburn ReliefChewscalcium carbonate	Calcium carbonate 750 mg/1	Tablet, ChewableOral	Bayer HealthCare LLC.	0280-0042
Alka-Seltzer Gold	Citric acid monohydrate 1000 mg/1 + 2 more ingredients	Tablet, EffervescentOral	Bayer HealthCare LLC.	0280-4100
Alka-Seltzer Heartburnanhydrous citric acid, sodium bicarbonate (heat-treated)	Citric acid monohydrate 1000 mg/1; Sodium bicarbonate 1940 mg/1	Tablet, EffervescentOral	Bayer HealthCare LLC.	0280-0047
Alka-Seltzer Heartburn Plus Gas ReliefChews Tropical Punchcalcium carbonate and simethicone	Dimethicone 80 mg/1; Calcium carbonate 750 mg/1	Tablet, ChewableOral	Bayer HealthCare LLC.	0280-0225
Alka-Seltzer Heartburn Relief Extra Strengthanhydrous citric acid, sodium bicarbonate (heat-treated)	Sodium bicarbonate 1976 mg/1; Citric acid monohydrate 1000 mg/1	Tablet, EffervescentOral	Bayer Healthcare LLC	0280-0079
Alka-Seltzer Heartburn Relief Lemon Limeanhydrous citric acid, sodium bicarbonate (heat-treated)	Sodium bicarbonate 1650 mg/1; Citric acid monohydrate 1000 mg/1	Tablet, EffervescentOral	Bayer Healthcare LLC	0280-0083
Alka-Seltzer Heartburn Relief Peppermintcalcium carbonate	Calcium carbonate 750 mg/1	Gum, ChewingOral	Bayer HealthCare LLC.	0280-0002
Alka-Seltzer Heartburn ReliefChewscalcium carbonate	Calcium carbonate 750 mg/1	Tablet, ChewableOral	Bayer HealthCare LLC.	0280-0221
Alka-Seltzer Heartburn ReliefChews Strawberry and Orangecalcium carbonate	Calcium carbonate 750 mg/1	Tablet, ChewableOral	Bayer HealthCare LLC.	0280-0224
Alka-Seltzer Kids Tummy ReliefChewscalcium carbonate and dimethicone	Calcium carbonate 750 mg/1; Dimethicone 80 mg/1	Tablet, ChewableOral	Bayer HealthCare LLC.	0280-0051
Alka-Seltzer Ultra Strength Heartburn ReliefChewscalcium carbonate	Calcium carbonate 1000 mg/1	Tablet, ChewableOral	Bayer HealthCare LLC.	0280-0245
Alka-Seltzer Ultra Strength Heartburn ReliefChews Strawberry and Orangecalcium carbonate	Calcium carbonate 1000 mg/1	Tablet, ChewableOral	Bayer HealthCare LLC.	0280-0059

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Lyophilized Amnion With Albumin (Human amniotic membrane) NDC 74458-238