Home NDC 49035-101-47 equate Ultra Strength Antacid
Product NDC 49035-101
Requested package NDC 49035-101-47
11-digit product format 490350101
Labeler code 49035
Product ID 49035-101_42216854-37c3-682e-e063-6394a90af153
Type HUMAN OTC DRUG
Nonproprietary name Antacid Tablets
Dosage form TABLET, CHEWABLE
Route ORAL
Labeler Wal-Mart Stores,Inc.,
Application M001
Marketing category OTC MONOGRAPH DRUG
Marketing start 2015-10-12
Substance CALCIUM CARBONATE
Active strength 1000 mg/1
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 · 3 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 49035-101 49035-101-47 I Inactivated by FDA excluded / ndc_excluded.zip fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 49035-101 49035-101-47 I Inactivated by FDA excluded / ndc_excluded.zip 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 49035-101 49035-101-47 I Inactivated by FDA excluded / ndc_excluded.zip bd6a592717d7…303034d00443…
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 equate Ultra Strength Antacid
Brand name suffix Peppermint Flavor
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CALCIUM CARBONATE 1000 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination H0G9379FGK Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 308892 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 49035-101-47 equate Ultra Strength AntacidPeppermint Flavor 160 in 1 BOTTLE, PLASTIC TABLET, CHEWABLE 160 7 49035-101-01 Hand Sanitizer Bodycology 30 mL in 1 BOTTLE GEL 30 3 49035-101-02 Hand Sanitizer Bodycology 1 in 1 BOTTLE GEL 1 3
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded ALCOHOL ACTIVE INGREDIENT 3K9958V90M HAND SANITIZER (ETHYL ALCOHOL) GEL [WAL-MART STORES, INC.] 3 ALCOHOL ACTIVE MOIETY 3K9958V90M HAND SANITIZER (ETHYL ALCOHOL) GEL [WAL-MART STORES, INC.] 3 ALOE VERA LEAF INACTIVE INGREDIENT ZY81Z83H0X HAND SANITIZER (ETHYL ALCOHOL) GEL [WAL-MART STORES, INC.] 3 CARBOMER INTERPOLYMER TYPE A (55000 MPA.S)) INACTIVE INGREDIENT 59TL3WG5CO HAND SANITIZER (ETHYL ALCOHOL) GEL [WAL-MART STORES, INC.] 3 D&C RED NO. 33 INACTIVE INGREDIENT 9DBA0SBB0L HAND SANITIZER (ETHYL ALCOHOL) GEL [WAL-MART STORES, INC.] 3 FD&C BLUE NO. 1 INACTIVE INGREDIENT H3R47K3TBD HAND SANITIZER (ETHYL ALCOHOL) GEL [WAL-MART STORES, INC.] 3 FD&C RED NO. 4 INACTIVE INGREDIENT X3W0AM1JLX HAND SANITIZER (ETHYL ALCOHOL) GEL [WAL-MART STORES, INC.] 3 FD&C YELLOW NO. 5 INACTIVE INGREDIENT I753WB2F1M HAND SANITIZER (ETHYL ALCOHOL) GEL [WAL-MART STORES, INC.] 3 GELATIN INACTIVE INGREDIENT 2G86QN327L HAND SANITIZER (ETHYL ALCOHOL) GEL [WAL-MART STORES, INC.] 3 PROPYLENE GLYCOL INACTIVE INGREDIENT 6DC9Q167V3 HAND SANITIZER (ETHYL ALCOHOL) GEL [WAL-MART STORES, INC.] 3 TROLAMINE INACTIVE INGREDIENT 9O3K93S3TK HAND SANITIZER (ETHYL ALCOHOL) GEL [WAL-MART STORES, INC.] 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 49035-101 EQUATE ULTRA STRENGTH ANTACID PEPPERMINT FLAVOR (ANTACID TABLETS) TABLET, CHEWABLE [WAL-MART STORES,INC.,] 6 Current NDC, Legacy NDC, 1 package rows 20241116_6a18cd92-cc51-401b-9074-fbaa1afb42ac.zip 49035-101 HAND SANITIZER (ETHYL ALCOHOL) GEL [WAL-MART STORES, INC.] 3 Current NDC, Legacy NDC, 2 package rows 20110413_3ca632ea-6404-4d91-bffc-7162aecb0ce5.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 8 of 34 · 678 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 49035-101-47 49035010147 160 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (49035-101-47) 2015-10-12 0000-00-00 No No Current