Dr. Talbots

Product NDC: 70797-160
11-digit product format: 707970160
Labeler code: 70797
Product ID: 70797-160_2b380620-3e8e-77b0-e063-6394a90a9442
Type: HUMAN OTC DRUG
Nonproprietary name: Ethyl Alcohol
Dosage form: GEL
Route: TOPICAL
Labeler: Talbot�s Pharmaceuticals Family Products, LLC.
Application: M014
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2020-05-29
Substance: ALCOHOL
Active strength: 75 mL/100mL
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

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: Dr. Talbots
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ALCOHOL	75 mL/100mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
3K9958V90M	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1305100	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
a6a94205-a9ff-7709-e053-2995a90a066b	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
70797-160-01	Dr. Talbots	50 mL in 1 BOTTLE	GEL	50	4
70797-160-02	Dr. Talbots	250 mL in 1 BOTTLE, PUMP	GEL	250	4
70797-160-03	Dr. Talbots	500 mL in 1 BOTTLE, PUMP	GEL	500	4
70797-160-04	Dr. Talbots	1000 mL in 1 BOTTLE, PUMP	GEL	1000	4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70797-160	DR. TALBOTS (ETHYL ALCOHOL) GEL [TALBOT&RSQUO;S PHARMACEUTICALS FAMILY PRODUCTS, LLC.]	4	Current NDC, Legacy NDC, 4 package rows	20250110_a6a94205-a9ff-7709-e053-2995a90a066b.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 7 of 7 · 129 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
EAR WAX RMVL Rite Aid	CARBAMIDE PEROXIDE 6.5%	Rite Aid	9e3cedcc-e523-2653-e053-2a95a90ad143	2023-12-15	Warnings	Exact identifier application number: M014
EarWax Removal Kit Rite Aid	CARBAMIDE PEROXIDE 6.5%	Rite Aid	da78ac58-6c1c-4fa9-baac-e9dec0241385	2023-12-15	Warnings	Exact identifier application number: M014
Otix Ear wax Removal System Ear wax and Bulb	CARBAMIDE PEROXIDE	Bell Pharmaceuticals, Inc.	15868798-28cd-4495-9baf-711e81ad8bdd	2023-12-14	Warnings	Exact identifier application number: M014
Otix Ear wax Removal Drops	CARBAMIDE PEROXIDE	Bell Pharmaceuticals, Inc.	0e70ab09-9360-4ab6-a1fe-6f82af392581	2023-12-14	Warnings	Exact identifier application number: M014
TopCare Earwax Removal Drops	CARBAMIDE PEROXIDE	Topco Associates LLC	c5b1ad0e-3712-40fd-afbe-54c0b5f1160b	2023-12-14	Warnings	Exact identifier application number: M014
DG Health Earwax Removal kit	CARBAMIDE PEROXIDE 6.5%	DOLLAR GENERAL CORPORATION	4b6fc00f-72d7-4675-9881-b763f27c06e3	2023-12-07	Warnings	Exact identifier application number: M014
Ear Wax Removal Drops Equate	CARBAMIDE PEROXIDE - 6.5%	WALMART STORES INC	33065ba2-5ce2-4db7-9d7a-d8aa2f38a90d	2023-12-04	Warnings	Exact identifier application number: M014
Good Neighbor Pharmacy Earwax Removal Drops	CARBAMIDE PEROXIDE	Proficient Rx LP	a131447b-a5a0-45cd-a59c-a9f719275baa	2023-12-01	Warnings	Exact identifier application number: M014
Ear Wax Removal Drops	CARBAMIDE PEROXIDE - 6.5%	Sheffield Pharmaceuticals LLC	aad7e2cd-cb28-423c-a441-eabe6516d40f	2022-12-06	Warnings	Exact identifier application number: M014

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
3K9958V90M	ALCOHOL	64-17-5	ALCOHOL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1305100	ethanol 75 % Topical Gel	PSN	a6a94205-a9ff-7709-e053-2995a90a066b	4
1305100	ethanol 0.75 ML/ML Topical Gel	SCD	a6a94205-a9ff-7709-e053-2995a90a066b	4
1305100	ethanol 75 % Topical Gel	SY	a6a94205-a9ff-7709-e053-2995a90a066b	4

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
70797-160-01	70797016001	50 mL in 1 BOTTLE (70797-160-01)	50 ml	2020-05-29	0000-00-00	No	No	Current
70797-160-02	70797016002	250 mL in 1 BOTTLE, PUMP (70797-160-02)	250 ml	2020-05-29	0000-00-00	No	No	Current
70797-160-03	70797016003	500 mL in 1 BOTTLE, PUMP (70797-160-03)	500 ml	2020-05-29	0000-00-00	No	No	Current
70797-160-04	70797016004	1000 mL in 1 BOTTLE, PUMP (70797-160-04)	1000 ml	2020-05-29	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Dr. Talbots - Talbot’s Pharmaceuticals Family Products, LLC.	Talbot’s Pharmaceuticals Family Products, LLC.	2025-01-08	HUMAN OTC DRUG LABEL	4