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 21 of 70 · 1,384 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Pure petroleum	WHITE PETROLATUM	Topco Associates LLC	3babe2cf-9e6c-4f22-940f-c1fdf489f1c7	2026-02-13	Warnings, Adverse reactions	Exact identifier application number: M016
Clear Anti Itch	PRAMOXINE HCL, ZINC ACETATE	Topco Associates LLC	8d3d1ff5-4868-495d-807c-e45aa2176f63	2026-02-13	Warnings, Adverse reactions	Exact identifier application number: M016
Healing	PETROLATUM	Topco Associates LLC	b929b159-4af5-4a03-8e7c-676a6ba2bf55	2026-02-13	Warnings, Adverse reactions	Exact identifier application number: M016
Calamine	CALAMINE, PRAMOXINE HCL	Topco Associates LLC	15d1ae3f-509c-4e6b-8f0c-cf9265680358	2026-02-13	Warnings, Adverse reactions	Exact identifier application number: M016
Petroleum	WHITE PETROLATUM	Topco Associates LLC	cd7f1727-0b6e-4993-9820-43783994efa1	2026-02-13	Warnings, Adverse reactions	Exact identifier application number: M016
Dimethicone	DIMETHICONE	Topco Associates LLC	f37f17f7-f084-4b74-8361-178d2315a476	2026-02-13	Warnings, Adverse reactions	Exact identifier application number: M016
Baby Eczema Therapy	COLLOIDAL OATMEAL	Topco Associates LLC	4f6af42c-f41e-455f-b94b-3793bf0b9a3f	2026-02-13	Warnings, Adverse reactions	Exact identifier application number: M016
Daily Moisturizing	DIMETHICONE	Topco Associates LLC	47e54eee-70e0-4bfa-ae77-d61a6560a9e1	2026-02-13	Warnings, Adverse reactions	Exact identifier application number: M016
Witch Hazel	WITCH HAZEL	Topco Associates LLC	471a9f8d-ba12-41d3-a510-20c1a13ff850	2026-02-13	Warnings, Adverse reactions	Exact identifier application number: M016
Skin Protectant	PETROLATUM	Wakefern Food Corp.	b799229b-f7ca-494c-afde-1fd096aef66e	2026-02-13	Warnings, Adverse reactions	Exact identifier application number: M016
Diaper Rash	ZINC OXIDE	WinCo Foods, LLC	659cc8c7-6300-41c0-a684-c5fde7f2b100	2026-02-12	Warnings, Adverse reactions	Exact identifier application number: M016
Zinc Oxide	ZINC OXIDE	Walgreen Co.	220f70e1-0802-4fe2-92d0-78dec557c993	2026-02-12	Warnings, Adverse reactions	Exact identifier application number: M016
Witch Hazel	WITCH HAZEL	Walgreen Co.	417ae199-54bb-420f-a3cf-1c096062d78c	2026-02-12	Warnings, Adverse reactions	Exact identifier application number: M016
First Aid Beauty Dry Skin Rescue Kit	COLLOIDAL OATMEAL	The Procter & Gamble Manufacturing Company	4a93d029-d721-0bb5-e063-6294a90a17c4	2026-02-11	Warnings	Exact identifier application number: M016
Natouch Eczema Wipes	ECZEMA WIPES	Natouch LLC	0a9756a4-2fa9-cd19-e063-6294a90a93ad	2026-02-10	Warnings	Exact identifier application number: M016
EARTHS CARE Eczema Cream	ECZEMA	DLC Laboratories, Inc.	17436fa0-d6c7-1052-e063-6294a90adae4	2026-02-09	Warnings	Exact identifier application number: M016
Petrolatum	WHITE PETROLATUM	Retail Business Services, LLC	bf0c9494-0138-4346-9348-e235ca4d9e58	2026-02-06	Warnings, Adverse reactions	Exact identifier application number: M016
Clear Anti-Itch	PRAMOXINE HCL, ZINC ACETATE	Retail Business Services, LLC	a80b8fee-2dd9-4640-a4f8-4cf940df8563	2026-02-06	Warnings, Adverse reactions	Exact identifier application number: M016
Advanced Healing	PETROLATUM	Retail Business Services, LLC	6e9121c8-5eb9-4d0b-86c5-b892e14bdab8	2026-02-06	Warnings	Exact identifier application number: M016
Petrolatum	WHITE PETROLATUM	Retail Business Services, LLC	bf73c618-ed2f-4468-a51f-ff61c7b1f506	2026-02-06	Warnings, Adverse reactions	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