Absorbine Jr.

Product NDC: 69693-411
11-digit product format: 696930411
Labeler code: 69693
Product ID: 69693-411_46a7d76e-bbab-cddc-e063-6294a90a5096
Type: HUMAN OTC DRUG
Nonproprietary name: Menthol
Dosage form: LIQUID
Route: TOPICAL
Labeler: Clarion Brands, LLC
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2010-06-24
Substance: MENTHOL
Active strength: 4 g/100mL
NDC exclude flag: No
Listing certified through: 2027-12-31
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: Absorbine Jr.
Brand name suffix: Plus
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MENTHOL	4 g/100mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
L7T10EIP3A	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
283438	Internal RxNorm lookup
751892	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
fd5d77fc-dc73-2aec-2c7f-0fca5d7d3a75	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
5f30b278-5791-4113-8781-878a9221ef8a	Product name	2	20230125
2a70c781-a755-4d76-b20a-a958acfbdcdc	Product name	2	20190619
304592ef-4a8a-4c22-8e8c-af73aa3d60e5	Product name	1	20180703
ac0821a1-ce75-4ea7-880a-59eecaecdf22	Product name	1	20180703
db5dc4f9-b907-46f6-8fb7-babcf04bbe5c	Product name	1	20180619
41e9d6cf-3ed7-4c44-a57e-0685058d0896	Product name	1	20170824
5e652c92-68fd-426b-b0e7-5fc64e0b9f99	Product name	1	20170309
ddc0c11a-bba8-408f-b3c7-c4828b4bcc8c	Product name	1	20150421

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
69693-411-04	Absorbine Jr.Plus	118 mL in 1 BOTTLE, WITH APPLICATOR	LIQUID	118		12
69693-411-04	Absorbine Jr.Plus	1 in 1 CARTON	LIQUID	1		12

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Menthol	ACTIVE INGREDIENT	L7T10EIP3A	ABSORBINE JR. PLUS (MENTHOL) LOTION [CLARION BRANDS, LLC]	1
Menthol	ACTIVE MOIETY	L7T10EIP3A	ABSORBINE JR. PLUS (MENTHOL) LOTION [CLARION BRANDS, LLC]	1
Acetone	INACTIVE INGREDIENT	1364PS73AF	ABSORBINE JR. PLUS (MENTHOL) LOTION [CLARION BRANDS, LLC]	1
Calendula Officinalis Flower	INACTIVE INGREDIENT	P0M7O4Y7YD	ABSORBINE JR. PLUS (MENTHOL) LOTION [CLARION BRANDS, LLC]	1
Echinacea, Unspecified	INACTIVE INGREDIENT	4N9P6CC1DX	ABSORBINE JR. PLUS (MENTHOL) LOTION [CLARION BRANDS, LLC]	1
Fd&c Blue No. 1	INACTIVE INGREDIENT	H3R47K3TBD	ABSORBINE JR. PLUS (MENTHOL) LOTION [CLARION BRANDS, LLC]	1
Iodine	INACTIVE INGREDIENT	9679TC07X4	ABSORBINE JR. PLUS (MENTHOL) LOTION [CLARION BRANDS, LLC]	1
Potassium Iodide	INACTIVE INGREDIENT	1C4QK22F9J	ABSORBINE JR. PLUS (MENTHOL) LOTION [CLARION BRANDS, LLC]	1
Thymol	INACTIVE INGREDIENT	3J50XA376E	ABSORBINE JR. PLUS (MENTHOL) LOTION [CLARION BRANDS, LLC]	1
Water	INACTIVE INGREDIENT	059QF0KO0R	ABSORBINE JR. PLUS (MENTHOL) LOTION [CLARION BRANDS, LLC]	1
Wormwood	INACTIVE INGREDIENT	F84709P2XV	ABSORBINE JR. PLUS (MENTHOL) LOTION [CLARION BRANDS, LLC]	1
Wormwood Oil	INACTIVE INGREDIENT	01756N87N8	ABSORBINE JR. PLUS (MENTHOL) LOTION [CLARION BRANDS, LLC]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
69693-411	ABSORBINE JR. PLUS (MENTHOL) LIQUID [CLARION BRANDS, LLC]	11	Current NDC, Legacy NDC, 2 package rows	20241225_fd5d77fc-dc73-2aec-2c7f-0fca5d7d3a75.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 130 of 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
TIDL PAIN RELIEF HEAT THERAPY ROLL-ON	PAIN RELIEF HEAT THERAPY ROLL-ON	Shenzhen Sam Technology Co., Ltd.	1d0b7b8f-9e5d-00f7-e063-6394a90af87c	2024-07-12	Warnings	Exact identifier application number: M017
TIDL PAIN RELIEF CRYO THERAPY original formula Spray.	PAIN RELIEF CRYO THERAPY ORIGINAL FORMULA SPRAY	Shenzhen Sam Technology Co., Ltd.	1d0b94ec-f956-dff2-e063-6294a90aca4a	2024-07-12	Warnings	Exact identifier application number: M017
TIDL PAIN RELIEF CRYO THERAPY MAX Strength Spray.	PAIN RELIEF CRYO THERAPY MAX STRENGTH SPRAY	Shenzhen Sam Technology Co., Ltd.	1d0bf4f9-6b02-6cec-e063-6294a90a36c7	2024-07-12	Warnings	Exact identifier application number: M017
Burn Relief	LIDOCAINE HCI 2.0%	Trifecta Pharmaceuticals USA, LLC.	e5e524cd-bb22-715f-e053-2995a90ab5d3	2024-07-12	Warnings	Exact identifier application number: M017
Ralli Rapid Pain Relief	MENTHOL	Troy Manufacturing, Inc.	1d10e3ca-dc93-8e1a-e063-6394a90a47c0	2024-07-12	Warnings	Exact identifier application number: M017
TIDL PAIN RELIEF HEAT THERAPY Spray.	PAIN RELIEF HEAT THERAPY SPRAY	Shenzhen Sam Technology Co., Ltd.	1d199826-1b27-b6e7-e063-6394a90a69ad	2024-07-12	Warnings	Exact identifier application number: M017
Tidl Pain Relief Morning Therapy Spray.	PAIN RELIEF MORNING THERAPY SPRAY	Shenzhen Sam Technology Co., Ltd.	1d19d070-3818-73de-e063-6394a90a8958	2024-07-12	Warnings	Exact identifier application number: M017
Hydrocortisone with aloe	HYDROCORTISONE WITH ALOE ANTI ITCH	NeilMed Pharmaceuticals Inc.	032b9f58-5f64-04dd-e063-6294a90a6bb9	2024-07-10	Warnings	Exact identifier application number: M017
Octagon Pain Relief	MENTHOL, UNSPECIFIED FORM	NATURAL ESSENTIALS, INC.	9926f733-1506-4224-9d70-b1813cd81ec3	2024-07-08	Warnings	Exact identifier application number: M017
LidoReal Patch	LIDOCAINE AND MENTHOL	FORREAL PHARMACEUTICALS LLC	19f1c037-b4b8-47b0-b0f9-036691c1d307	2024-07-05	Warnings	Exact identifier application number: M017
Lip Medex Lip Balm	PETROLATUM, CAMPHOR (SYNTHETIC), MENTHOL, UNSPECIFIED FORM, AND PHENOL	Blistex Inc.	988f97e8-a59f-4bc0-9d71-60607364a686	2024-07-01	Warnings	Exact identifier application number: M017
Maybelline New York BABY LIPS DR RESCURE MENTHOL EXTERNAL ANALGESIC MEDICATED BALM	MENTHOL	L'Oreal USA Products Inc	d580982f-dda6-4b03-bf84-342b9f2c6d93	2024-06-29	Warnings	Exact identifier application number: M017
Lip Medex Cherry	PETROLATUM, CAMPHOR (SYNTHETIC), AND MENTHOL, UNSPECIFIED FORM	Blistex Inc.	fa8b3fb1-08e5-4876-9c4a-6aa8c9f23af8	2024-06-28	Warnings	Exact identifier application number: M017
10% Methyl Salicylate Pain Relief Patch	10% METHYL SALICYLATE	Akron Coating & Adhesives	1be1f1ce-3238-a8ed-e063-6294a90a5aed	2024-06-27		Exact identifier application number: M017
Genuine First Aid Alcohol Cleansing Pad	BENZOCAINE, ALCOHOL	GFA Production (Xiamen) Co., Ltd.	c39c4d80-9718-459f-8ae4-ada043bba5b7	2024-06-26	Warnings	Exact identifier application number: M017
Eagle Brand Medicated Roll On	MENTHOL, METHYL SALICYLATE	PT. EAGLE INDO PHARMA	1bd5cf69-9a08-5e2e-e063-6394a90a03cd	2024-06-26	Warnings	Exact identifier application number: M017
Solarcaine Burn Pain Relief 4oz	SOLARCAINE BURN PAIN RELIEF 4OZ	WellSpring Pharmaceutical Corporation	2c0389db-ceb2-422b-9575-bdb8fe649a1e	2024-06-26	Warnings	Exact identifier application number: M017
astonea	HYDROCORTISONE	ASTONEA LABS PRIVATE LIMITED	de09e859-c5fd-0cc5-e053-2a95a90a147e	2024-06-25	Warnings	Exact identifier application number: M017
HealthWise Pain Relief Lidocaine Patch	LIDOCAINE 4%	Veridian Healthcare	0190196d-5f78-042b-e063-6294a90a3714	2024-06-25	Warnings	Exact identifier application number: M017
Eagle Brand Medicated Oil	MENTHOL, METHYL SALICYLATE	PT. EAGLE INDO PHARMA	1bc1bf83-91ee-ec9d-e063-6394a90a3daf	2024-06-25	Warnings	Exact identifier application number: M017

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
751892	Absorbine Jr. Extra Strength 4 % Topical Solution	PSN	fd5d77fc-dc73-2aec-2c7f-0fca5d7d3a75	12
283438	menthol 4 % Topical Solution	PSN	fd5d77fc-dc73-2aec-2c7f-0fca5d7d3a75	12
751892	menthol 40 MG/ML Topical Solution [Absorbine Jr.]	SBD	fd5d77fc-dc73-2aec-2c7f-0fca5d7d3a75	12
283438	menthol 40 MG/ML Topical Solution	SCD	fd5d77fc-dc73-2aec-2c7f-0fca5d7d3a75	12
751892	Absorbine Jr. Extra Strength 4 % Topical Solution	SY	fd5d77fc-dc73-2aec-2c7f-0fca5d7d3a75	12
751892	Absorbine Jr. Extra Strength 40 MG/ML Topical Solution	SY	fd5d77fc-dc73-2aec-2c7f-0fca5d7d3a75	12
283438	menthol 4 % Topical Solution	SY	fd5d77fc-dc73-2aec-2c7f-0fca5d7d3a75	12

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
69693-411-04	69693041104	1 BOTTLE, WITH APPLICATOR in 1 CARTON (69693-411-04) / 118 mL in 1 BOTTLE, WITH APPLICATOR	2010-06-24	0000-00-00	No	No	Current