Scar Reducer

Product NDC: 70084-710
11-digit product format: 700840710
Labeler code: 70084
Product ID: 70084-710_40838898-6268-702c-e063-6394a90a8b3d
Type: HUMAN OTC DRUG
Nonproprietary name: Allantoin
Dosage form: CREAM
Route: TOPICAL
Labeler: Quantum, Inc
Application: M016
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2021-10-25
Substance: ALLANTOIN
Active strength: 1 g/100g
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 16 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Code	Status	Snapshot	Source SHA-256
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	70084-710-01	I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	70084-710-01	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	70084-710-01	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	70084-710-01	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	70084-710-01	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	70084-710-01	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	70084-710-01	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	70084-710-01	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product: Yes
Brand name base: Scar Reducer
Brand name suffix: Intensive Herbal and Nutrient
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ALLANTOIN	1 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
344S277G0Z	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
2001650	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
5197f1fa-aae5-406c-97d9-635b8c1a88a8	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
ebc62596-fc97-4d03-9483-7ba095d25db7	Product name	1	20151210
0ca1d589-929b-4b33-bc5b-1d84abdafa6a	Product name	1	20150324
fc363c46-397b-4476-ac0f-70e43e8e4592	Product name	1	20150324
60c52429-fcef-eb54-2387-43bc9e4f296b	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
Effective	Related label
2025-01-30	Scar Reducer Intensive Herbal & Nutrient
2025-01-30	Scar Reducer Intensive Herbal & Nutrient
2023-02-09	Scar Reducer Intensive Herbal & Nutrient
2023-02-09	Scar Reducer Intensive Herbal & Nutrient
2023-01-30	Scar Reducer Intensive Herbal & Nutrient
2023-01-30	Scar Reducer Intensive Herbal & Nutrient

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70084-710-01	Scar ReducerIntensive Herbal and Nutrient	1 in 1 BOX	CREAM	1		3
70084-710-01	Scar ReducerIntensive Herbal and Nutrient	21 g in 1 TUBE	CREAM	21		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70084-710	SCAR REDUCER INTENSIVE HERBAL AND NUTRIENT (ALLANTOIN) CREAM [QUANTUM, INC]	2	Current NDC, Legacy NDC, 2 package rows	20230210_5197f1fa-aae5-406c-97d9-635b8c1a88a8.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 40 of 68 · 1,357 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
EIGHT HOUR SKIN FRAGRANCE FREE	PETROLATUM	REVLON	b61d6e2e-18dd-37d2-e053-2a95a90af57b	2025-08-01	Warnings	Exact identifier application number: M016
Vigority Wild Yam Cream	ESTRIOL CREAM	FOUNDATION COMMERCE INC	39b2bef7-46c5-9ad5-e063-6294a90ae983	2025-07-30	Warnings	Exact identifier application number: M016
Rugby Caldyphen Clear	PRAMOXINE HYDROCHLORIDE AND ZINC ACETATE LOTION	Rugby Laboratories	9af3a740-ef97-26ce-e053-2a95a90a0ee1	2025-07-28	Warnings	Exact identifier application number: M016
Aveeno Baby Eczema Therapy Soothing Bath Treatment	OATMEAL	Kenvue Brands LLC	e7eb10b7-3950-49cb-ba73-11e7581b6be9	2025-07-25	Warnings	Exact identifier application number: M016
ProCure SkinGuard	PETROLATUM 49.9%	Twin Med LLC	3a1721f6-1bb0-cd47-e063-6394a90a148e	2025-07-25	Warnings	Exact identifier application number: M016
ProCure HydroCerin	PETROLATUM 33%	Twin Med LLC	3ab7248d-b914-9fdd-e063-6294a90ac4c8	2025-07-24	Warnings	Exact identifier application number: M016
AD PREVENT Original	AD PREVENT ORIGINAL	WellSpring Pharmaceutical Corporation	cf73246e-81c1-42e9-a107-dc6c99cf7d01	2025-07-24	Warnings	Exact identifier application number: M016
Dimethicone 1 Skin Protectant	DIMETHICONE	Universal Distribution Center LLC	2c5b96b9-24d6-4223-a63d-fe83d7c02368	2025-07-24	Warnings	Exact identifier application number: M016
Dr Butlers Soothing Incontinence	MINERAL OIL 59.8%, PETROLATUM 36.0%	Beyond Health PA	3a9d3796-fd05-fe57-e063-6294a90a0ac6	2025-07-23	Warnings	Exact identifier application number: M016
A and D plus E	VITAMIN A, D AND E OINTMENT	Derma Sciences Canada Inc.	35aca592-bfd0-652f-e063-6394a90ac53e	2025-07-22	Warnings	Exact identifier application number: M016
Petroleum Jelly	PETROLATUM	Derma Sciences Canada Inc.	3a895e6c-da8d-db9b-e063-6394a90ace40	2025-07-22	Warnings	Exact identifier application number: M016
Petroleum Jelly	PETROLEUM JELLY	NeilMed Pharmaceuticals Inc.	36bbbb1e-78e9-98f6-e063-6294a90a66d1	2025-07-21	Warnings	Exact identifier application number: M016
Mountain Ice Eczema	COLLOIDAL OATMEAL	Mountainside Medical Equipment, Inc.	1a91f33e-dd85-4d5a-b61c-e460a507e292	2025-07-21	Warnings	Exact identifier application number: M016
Our Eczema Remedy	COLLOIDAL OATMEAL	Fewer Better Things	3a755b4c-47c8-9ca5-e063-6394a90af84a	2025-07-21	Warnings	Exact identifier application number: M016
Aveeno DAILY MOISTURIZING	DIMETHICONE	Kenvue Brands LLC	54a13b85-32b5-439d-a27a-8fba2cf44251	2025-07-16	Warnings	Exact identifier application number: M016
ProCure Moisture Barrier	1% DIMETHICONE, 12% ZINC OXIDE	Twin Med LLC	3988c83b-d4eb-1f09-e063-6394a90a45ad	2025-07-14	Warnings	Exact identifier application number: M016
Avalon Organics Antidandruff Conditioner	SALICYLIC ACID	The Hain Celestial Group, Inc.	66db1071-022a-aa19-e053-2a91aa0a8e39	2025-07-11	Warnings	Exact identifier application number: M016
Avalon Organics Antidandruff	SALICYLIC ACID	The Hain Celestial Group, Inc.	66c7f730-64f3-4eef-e053-2a91aa0a4225	2025-07-11	Warnings	Exact identifier application number: M016
terrasil Infection Protection Wound Care Maximum Strength	ALLANTOIN	Aidance Scientific, Inc, DBA Aidance Skincare & Topical Solutions	9e7843e2-ca69-40f5-a4ce-da6b03ebe7f7	2025-07-11	Warnings	Exact identifier application number: M016
terrasil Skin Repair	ALLANTOIN	Aidance Scientific, Inc, DBA Aidance Skincare & Topical Solutions	92a23c7f-6b89-49cb-93e2-49ab7a85c86d	2025-07-11	Warnings	Exact identifier application number: M016

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
344S277G0Z	ALLANTOIN	97-59-6	ALLANTOIN

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
2001650	allantoin 1 % Topical Cream	PSN	5197f1fa-aae5-406c-97d9-635b8c1a88a8	3
2001650	allantoin 10 MG/ML Topical Cream	SCD	5197f1fa-aae5-406c-97d9-635b8c1a88a8	3
2001650	allantoin 1 % Topical Cream	SY	5197f1fa-aae5-406c-97d9-635b8c1a88a8	3

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
70084-710-01	70084071001	1 TUBE in 1 BOX (70084-710-01) / 21 g in 1 TUBE	1 tube	2021-10-25	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Scar Reducer Intensive Herbal & Nutrient	Quantum, Inc \| SunDeep Corp	2025-10-06	HUMAN OTC DRUG LABEL	3