Airmit Ace

Product NDC: 49873-802
11-digit product format: 498730802
Labeler code: 49873
Product ID: 49873-802_0b7d81d6-f5ac-a151-e063-6294a90a8322
Type: HUMAN OTC DRUG
Nonproprietary name: dimenhydrinate
Dosage form: TABLET
Route: ORAL
Labeler: Sato Pharmaceutical Co., Ltd.
Application: M009
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2005-03-11
Substance: DIMENHYDRINATE
Active strength: 25 mg/1
Pharmacologic classes: Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
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: Airmit Ace
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
DIMENHYDRINATE	25 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
JB937PER5C	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
198602	Internal RxNorm lookup
1241485	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
a98d252d-4cfa-496a-ab2c-627f45f0d7d9	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
0e2e0f88-b076-afe1-4bdd-32bca4375bec	Product name	3	20250127
3e48c9c4-918d-5d23-2f0b-d2398b06be54	Product name	1	20140508
865c72dd-0d94-daac-f728-ddd4ded2a79e	Product name	1	20140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
49873-802-01	Airmit Ace	1 in 1 CARTON	TABLET	1		5
49873-802-01	Airmit Ace	6 in 1 BLISTER PACK	TABLET	6		5

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
dimenhydrinate	ACTIVE INGREDIENT	JB937PER5C	AIRMIT ACE (DIMENHYDRINATE) TABLET [SATO PHARMACEUTICAL CO., LTD.]	2
dimenhydrinate	ACTIVE MOIETY	JB937PER5C	AIRMIT ACE (DIMENHYDRINATE) TABLET [SATO PHARMACEUTICAL CO., LTD.]	2
CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS	INACTIVE INGREDIENT	L11K75P92J	AIRMIT ACE (DIMENHYDRINATE) TABLET [SATO PHARMACEUTICAL CO., LTD.]	2
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	AIRMIT ACE (DIMENHYDRINATE) TABLET [SATO PHARMACEUTICAL CO., LTD.]	2
FD&C YELLOW NO. 6	INACTIVE INGREDIENT	H77VEI93A8	AIRMIT ACE (DIMENHYDRINATE) TABLET [SATO PHARMACEUTICAL CO., LTD.]	2
HYDROXYPROPYL CELLULOSE	INACTIVE INGREDIENT	RFW2ET671P	AIRMIT ACE (DIMENHYDRINATE) TABLET [SATO PHARMACEUTICAL CO., LTD.]	2
HYDROXYPROPYL CORN STARCH (5% SUBSTITUTION BY WEIGHT)	INACTIVE INGREDIENT	9M44R3409A	AIRMIT ACE (DIMENHYDRINATE) TABLET [SATO PHARMACEUTICAL CO., LTD.]	2
LACTOSE	INACTIVE INGREDIENT	J2B2A4N98G	AIRMIT ACE (DIMENHYDRINATE) TABLET [SATO PHARMACEUTICAL CO., LTD.]	2
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	AIRMIT ACE (DIMENHYDRINATE) TABLET [SATO PHARMACEUTICAL CO., LTD.]	2
MANNITOL	INACTIVE INGREDIENT	3OWL53L36A	AIRMIT ACE (DIMENHYDRINATE) TABLET [SATO PHARMACEUTICAL CO., LTD.]	2
POVIDONE	INACTIVE INGREDIENT	FZ989GH94E	AIRMIT ACE (DIMENHYDRINATE) TABLET [SATO PHARMACEUTICAL CO., LTD.]	2
SUCROSE	INACTIVE INGREDIENT	C151H8M554	AIRMIT ACE (DIMENHYDRINATE) TABLET [SATO PHARMACEUTICAL CO., LTD.]	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
49873-802	AIRMIT ACE (DIMENHYDRINATE) TABLET [SATO PHARMACEUTICAL CO., LTD.]	5	Current NDC, Legacy NDC, 2 package rows	20231203_a98d252d-4cfa-496a-ab2c-627f45f0d7d9.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 6 of 6 · 112 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Gravol	DIMENHYDRINATE	Church & Dwight Co., Inc.	d941705f-12a1-4757-e053-2995a90ad3fa	2024-05-13	Warnings	Exact identifier application number: M009
Kids Gravol Chewables Motion Sickness Dimenhydrinate	DIMENHYDRINATE	Church & Dwight Co., Inc.	cf6de950-a157-4be2-a302-0dc19511d2f2	2024-03-01	Warnings	Exact identifier application number: M009
Gravol Chewables Motion Sickness Dimenhydrinate	DIMENHYDRINATE	Church & Dwight Co., Inc.	de5249f7-79fc-4f3c-965a-1e8ec978a0b7	2024-03-01	Warnings	Exact identifier application number: M009
Meclizine HCl	MECLIZINE HYDROCHLORIDE CHEWABLE	BluePoint Laboratories	d9cc2705-9dcc-0a73-e053-2995a90aafe6	2024-02-21	Warnings	Exact identifier application number: M009
Childrens Allergy	DIPHENHYDRAMINE HYDROCHLORIDE	DeMoulas Market Basket	fd04fb94-f581-4ca2-b7ac-20359093863e	2023-12-29	Warnings	Exact identifier application number: M009
Airmit Ace	DIMENHYDRINATE	Sato Pharmaceutical Co., Ltd.	a98d252d-4cfa-496a-ab2c-627f45f0d7d9	2023-12-01	Warnings	Exact identifier application number: M009 ndc (product): 49873-802
Meclizine HCl	MECLIZINE HYDROCHLORIDE	BluePoint Laboratories	d9cae5a6-8d4b-bdaf-e053-2995a90a7d44	2023-11-17	Warnings	Exact identifier application number: M009
ZenTrip Motion Sickness	MECLIZINE HYDROCHLORIDE	Sato Pharmaceutical Co., LTD	bd86c4c7-b6f0-e3e8-e053-2995a90a4454	2023-11-03	Warnings	Exact identifier application number: M009
Travel-Ease	MECLIZINE HCL	Geri-Care Pharmaceutical Corp	e3c64eb9-4972-29d9-e053-2a95a90a2a8a	2023-10-25	Warnings	Exact identifier application number: M009
Gravol	DIMENHYDRINATE	Church & Dwight Co., Inc.	d95240bb-02f2-3226-e053-2995a90afacd	2022-03-03	Warnings	Exact identifier application number: M009
Allergy DyeFree	ALLERGY DYEFREE	Allegiant Health	15736bb8-5a5b-489d-83ad-4cf34ec62956	2021-04-26	Warnings	Exact identifier application number: M009
Motion Sickness Relief	DIMENHYDRINATE 50MG	Allegiant Health	7b0aa993-f08f-4dff-a82d-f35b3ebe3cc1	2019-12-12	Warnings	Exact identifier application number: M009

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
JB937PER5C	DIMENHYDRINATE	523-87-5	DIMENHYDRINATE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1241485	Airmit Ace 25 MG Oral Tablet	PSN	a98d252d-4cfa-496a-ab2c-627f45f0d7d9	5
198602	dimenhyDRINATE 25 MG Oral Tablet	PSN	a98d252d-4cfa-496a-ab2c-627f45f0d7d9	5
1241485	dimenhydrinate 25 MG Oral Tablet [Airmit]	SBD	a98d252d-4cfa-496a-ab2c-627f45f0d7d9	5
198602	dimenhydrinate 25 MG Oral Tablet	SCD	a98d252d-4cfa-496a-ab2c-627f45f0d7d9	5
1241485	Airmit 25 MG Oral Tablet	SY	a98d252d-4cfa-496a-ab2c-627f45f0d7d9	5

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
49873-802-01	49873080201	1 BLISTER PACK in 1 CARTON (49873-802-01) / 6 TABLET in 1 BLISTER PACK	1 blister pack	2005-03-11	0000-00-00	No	No	Current