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
365 Whole Foods Market Epsom Saltmagnesium sulfate	Magnesium sulfate heptahydrate 1 g/g	Granule, For solutionOral, Topical	Whole Foods Market, Inc.	42681-0060
4718 Enema, Mineral Oil	Mineral oil 133 g/133mL	EnemaRectal	Dynarex	67777-430
Acetaminophenextra strength pain relief	Acetaminophen 500 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-5239
Alcohol wet wipes	Alcohol 75 mL/100mL	DressingTopical	Shandong Aishule Hygiene Products Co., Ltd	82061-006
Amazon Fiber Capletscalcium polycarbophil	Calcium polycarbophil 625 mg/1	Tablet, Film coatedOral	AMAZON.COM SERVICES LLC	72288-201
Amazon Fiber Therapymethylcellulose	Methylcellulose (4000 mpa.s) 500 mg/1	TabletOral	AMAZON.COM SERVICES LLC	72288-122
Anecream 5lidocaine 5%	Lidocaine 5 g/100g	CreamTopical	Focus Health Group	24357-702
basic care stool softenerdocusate sodium	Docusate sodium 100 mg/1	Capsule, Liquid filledOral	Amazon.com Services LLC	72288-486
Best Choicecalcium polycarbophil	Calcium polycarbophil 625 mg/1	Tablet, Film coatedOral	BEST CHOICE (VALU MERCHANDISERS COMPANY)	63941-023
Best Choice Fiber Laxativepsyllium husk	Psyllium husk .52 g/1	CapsuleOral	BEST CHOICE (VALU MERCHANDISERS COMPANY)	63941-119
Best Choice Fiber Therapymethylcellulose	Methylcellulose (4000 mpa.s) 500 mg/1	TabletOral	BEST CHOICE (VALU MERCHANDISERS COMPANY)	63941-122
Best Choice Fiber Therapy Orange Flavorpsyllium husk	Psyllium husk 3.4 g/12g	PowderOral	BEST CHOICE (VALU MERCHANDISERS COMPANY)	63941-513
Best Choice Fiber Therapy original coarsepsyllium husk	Psyllium husk 3.4 g/7g	PowderOral	BEST CHOICE (VALU MERCHANDISERS COMPANY)	63941-511
Bisacodyl	Bisacodyl 10 mg/1	SuppositoryRectal	Padagis US LLC	0574-7050
Bisacodyl	Bisacodyl 10 mg/1	SuppositoryRectal	Major Pharmaceuticals	0904-7142
Bisacodylbiscodyl	Bisacodyl 5 mg/1	Tablet, CoatedOral	TARGET CORPORATION	11673-182
Bisacodyl	Bisacodyl 5 mg/1	Tablet, CoatedOral	KROGER COMPANY	41226-003
Bisacodyl	Bisacodyl 10 mg/1	SuppositoryRectal	Rising Pharma Holdings, Inc.	57237-327
Bisacodyl	Bisacodyl 10 mg/1	SuppositoryRectal	Pharmacy Value Alliance LLC	68016-084
Bisacodyl	Bisacodyl 10 mg/1	SuppositoryRectal	CVS Pharmacy	69842-816

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