What is NDC 30142-714?

30142-714 is the product NDC for Sunscreen, Avobenzone 30 mg/mL + 3 more ingredients lotion, listed with the FDA by The Kroger Co.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Sunscreen (Avobenzone, Homosalate, Octisalate, Octocrylene).

What is the active ingredient?

Avobenzone, Homosalate, Octisalate, Octocrylene.

The Kroger Co., NDC labeler code 30142. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Sunscreen?

25 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Sunscreen NDC 30142-714 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)30142-714Labeler and product segments. Claims need a package NDC.

Product NDC at billing width30142-0714Add 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
30142-714-34	3014207143430142071434	236 mL in 1 BOTTLE, PLASTIC (30142-714-34)Marketed from Nov 28, 2016

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): Sunscreen
Generic name (nonproprietary): avobenzone, homosalate, octisalate, octocrylene
Active ingredients: Avobenzone — 30 mg/mLHomosalate — 100 mg/mLOctisalate — 50 mg/mLOctocrylene — 100 mg/mL
Dosage form: Lotion
Route: Topical
Labeler: The Kroger Co.NDC labeler code 30142
Product type: Over-the-counter drug
Marketing category: OTC monograph drugApplication M 007
Marketing start: Nov 28, 2016
Listing expires: Dec 31, 2027
Identifiers: Product ID 30142-714_4bd1a6eb-2184-38d5-e063-6294a90a8bcbSPL ID 4bd1a6eb-2184-38d5-e063-6294a90a8bcbSPL set ID 3ae7e275-7bbc-4e62-b30f-013c40a89949UNII G63QQF2NOX, V06SV4M95S, 4X49Y0596W, 5A68WGF6WM

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

N430142071434 followed by a unit qualifier and the quantity

Package 30142-0714-34. 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 Feb 27, 2026.

Indications (excerpt from the label)

Uses helps prevent sunburn if used as directed with other sun protections measures (see Directions ), decreases the rist of skin cancer and early skin aging caused by the sun

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 30142-714

What is NDC 30142-714?: 30142-714 is the product NDC for Sunscreen, Avobenzone 30 mg/mL + 3 more ingredients lotion, listed with the FDA by The Kroger Co.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Sunscreen (Avobenzone, Homosalate, Octisalate, Octocrylene).
What is the active ingredient?: Avobenzone, Homosalate, Octisalate, Octocrylene.
Who is the labeler?: The Kroger Co., NDC labeler code 30142. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Sunscreen?: 25 other product NDCs are listed under this name. See all Sunscreen NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Sunscreen NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Sunscreenbroad spectrum spf 30	Octocrylene 5 g/100g + 2 more ingredients	SprayTopical	Charleston Dermatology, P.C.	87901-3019	87901-3019-01
Sunscreenbroad spectrum spf 30	Octocrylene 5 g/100g + 2 more ingredients	SprayTopical	1226 W AESTHETICS	82031-3019	82031-3019-01
Sunscreenbroad spectrum spf 30	Octocrylene 5 g/100g + 2 more ingredients	SprayTopical	Concierge Choice LLC	87955-3019	87955-3019-01
Sunscreenbroad spectrum spf 30	Octocrylene 5 g/100g + 2 more ingredients	SprayTopical	SKNVCARE, LLC	82704-3019	82704-3019-01
sunscreentitanium dioxide	Titanium dioxide 2.85 g/100mL; Ethylhexyl salicylate 3 g/100mL	LotionCutaneous	Guangdong Zhoubang Biotechnology Co., Ltd	87357-001	87357-0001-01
Sunscreenjapanese sunscreen spf 50 super water gel sunscreen 4.22floz(125g) refill	Octinoxate 1 g/1	CreamCutaneous	MAIDORA CO.,LTD	87243-123	87243-0123-35
sunscreentitanium dioxide(nano)	Titanium dioxide 4 g/100g; Ethylhexyl methoxycinnamate 7.5 g/100g	LotionTopical	Mingyu (guangdong) Cosmetics Technology Co., Ltd	87091-001	87091-0001-01
Sunscreen	Avobenzone 30 mg/mL + 2 more ingredients	LotionTopical	Old East Main Co.	75712-950	75712-0950-30
Sunscreentitanium dioxide 6.8%	Titanium dioxide .068 g/mL	LiquidTopical	Baxter of California, LLC	84203-001	84203-0001-01
Sunscreenavobenzone, homosalate, octisalate	Avobenzone 30 mg/g + 2 more ingredients	SprayTopical	Retail Business Services, LLC	72476-949	72476-0949-14

All 26 Sunscreen NDCs

Other NDCs under M 007

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

FDA NDC Directory listings under M 007
Product	Strength	Form · route	Labeler	Product NDC
Stool Softenerdocusate sodium	Docusate sodium 100 mg/1	Capsule, Liquid filledOral	Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)	55910-938
Glycerin	Glycerin 1 g/1	SuppositoryRectal	Chain Drug Consortium LLC	68016-161
Bisacodyl	Bisacodyl 10 mg/1	SuppositoryRectal	CVS Pharmacy	69842-816
Mineral oil	Mineral oil 100 mg/100mL	OilOral	EQUATE (Wal-Mart Stores, Inc.) (see also WAL-MART INC)	49035-035
Epsom Saltmagnesium sulfate	Magnesium sulfate, Unspecified 1 g/g	GranuleOral, Topical	Whole Foods Market	42681-6412
Stratuscare Glycerin Laxative Pediatricglycerin	Glycerin 1 g/1	SuppositoryRectal	Stratus Pharmaceuticals	58980-409
Senokotstandardized senna concentrate	Sennosides 8.6 mg/1	TabletOral	Atlantis Consumer Healthcare, Inc.	67618-300
Senna	Sennosides a and b 8.8 mg/5mL	SolutionOral	Rugby Laboratories	0536-1483
Milk Of Magnesia Cherrymagnesium hydroxide	Magnesium hydroxide 1200 mg/15mL	LiquidOral	TOP CARE (TOPCO ASSOCIATES LLC)	36800-684
Epsom Saltmagnesium sulfate	Magnesium sulfate, Unspecified 1 g/g	GranuleOral, Topical	Whole Foods Market	42681-6413
Stratuscare Adult Glyceringlycerin	Glycerin 2 g/1	SuppositoryRectal	Stratus Pharmaceuticals	58980-410
Phillips Fresh Mint Milk Of Magnesia	Magnesium hydroxide 1200 mg/15mL	LiquidOral	Bayer HealthCare LLC.	0280-0031
Senokot-Sstandardized senna concentrate and docusate sodium	Sennosides 8.6 mg/1; Docusate sodium 50 mg/1	TabletOral	Atlantis Consumer Healthcare, Inc.	67618-310
Senexon-Sdocusate sodium 50mg and sennosides 8.6mg	Sennosides 8.6 mg/1; Docusate sodium 50 mg/1	Tablet, Film coatedOral	RUGBY LABORATORIES	0536-1247
Equate Kids Gentle Laxative SCmagnesium hydroxide	Magnesium hydroxide 1200 mg/1	Tablet, ChewableOral	Walmart	79903-252
Stratuscare Bisacodylbisacodyl	Bisacodyl 10 mg/1	SuppositoryRectal	Stratus Pharmaceuticals	58980-415
Epsom Saltmagnesium sulfate	Magnesium sulfate heptahydrate 1 g/g	Granule, For solutionOral, Topical	Vi-Jon, LLC	0869-0602
Fleetbisacodyl	Bisacodyl 5 mg/1	Tablet, CoatedOral	C.B. Fleet Company, Inc.	0132-0401
Stool Softenerdocusate sodium	Docusate sodium 100 mg/1	TabletOral	Geri-Care Pharmaceuticals, Corp	57896-421
Stool Softener Extra Strengthdocusate sodium	Docusate sodium 250 mg/1	Capsule, Liquid filledOral	CVS Pharmacy	69842-740

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